Product approval
A certificate or approval attached to the finished product, component, or radio host.
Free · No signup · Official source linksDoes my medical device need TRC type approval of radiocommunication, telecommunication and ICT equipment in Cambodia?
Describe your device to check whether TRC type approval of radiocommunication, telecommunication and ICT equipment may apply, why, what facts are missing, and which official source to review.
1 maintained routes1 official source links
Preliminary applicability · country-specific scope
What you receive
Not just a yes or no
A route-by-route answer. Separate product certificates, dossier evidence, import documents, and facility licences stay separate.
Trigger reasoning. See which product facts matter and which missing facts prevent a reliable conclusion.
Official starting points. Open the regulator or government sources behind the maintained country matrix.
Maintained country rule
What this TRC type approval of radiocommunication, telecommunication and ICT equipment check is screening
Checks Wi-Fi, Bluetooth, cellular, NFC, RFID, UWB, telemetry, and proprietary radio approval. Maintained as a mandatory pre-market route.
Source association reviewed. The source association has been reviewed. This does not verify every rule, date or product-specific conclusion; read the cited provisions and their limits.
- Requirement family
- Radio and spectrum approval
- Regulatory object
- radiocommunication telecommunication or ict equipment
- Maintained rule status
- mandatory pre market
- Useful product facts
- Radio technologies, bands, power, antenna, module model, approval IDs, and host integration changes.
All radiocommunication, telecommunication and ICT equipment and devices require Type Approval before import and use in Cambodia. The duty is Article 16(b) of the Law on Telecommunications, promulgated by Royal Kram No. នស/រកម/1215/017 dated 17 December 2015, and Article 7(b) of Sub-Decree No. 110 ANK/BK dated 21 July 2017 on Granting Permit for Information and Communication Technology Operations; the certificate is issued per model by the Telecommunication Regulator of Cambodia, an entity attached to the Ministry of Post and Telecommunications, and Prakas No. 208 dated 29 December 2010 on Certification of Type Approval for Radiocommunications and Telecommunications Equipment sets the certification basis. Cambodia's own notification reports approval within 15 business days and a certificate valid for the lifetime of the model. It applies to a medical device only where the device is radiocommunication, telecommunication or ICT equipment — a wireless monitor, a telemetry module, a device with a cellular or Wi-Fi radio — and it is not the Department of Drugs and Food registration.
How to read the answer
Classification is only the first layer
A device may have one medical risk class and still trigger separate radio, electrical, measurement, radiation, environmental, import, or installation requirements. The checker keeps each regulatory object separate.
Dossier or import evidence
Testing can belong inside the medical dossier, while some documents apply to each shipment.
Site or operator licence
Radiation, installation, use, or measurement controls may apply to a facility or operator.
Country-specific scope
Other Cambodia routes to check
Telecom terminal
TRC qualified-agent certificate for importation, supply and distribution
Handled as an import or shipment-level obligation.
Source association reviewed
Import CoC / PVoC
TRC import permit for restricted radiocommunication and ICT goods
Handled as an import or shipment-level obligation.
Source association reviewed
EMC
EMC test evidence inside the TRC type-approval file
Applies when the product, feature, component, or use is in scope.
Source association reviewed
Electrical safety
Electrical-safety and performance evidence inside the AMDD dossier
Evidence is normally handled inside the medical-device registration route.
Source association reviewed
Radiation
MME/DONST licence and import permit for radioactive sources and ionizing-radiation equipment
Applies to the facility, operator, or installation rather than only the product.
Source association reviewed
Reviewed source associations
Use these authority pages to confirm current scope, technical rules, application routes, and transition dates. A linked source does not turn a preliminary result into an authority decision.
About this checker
A preliminary tool, not a regulatory determination
Describe the complete product — radio, power, measurement, radiation, battery, materials, accessories, intended use, import route, and existing approvals. The free checker maps those facts to the maintained Cambodia scheme matrix and links each route to its maintained source associations, with reviewed, candidate and unresolved states shown separately.
Use the result to identify questions and official sources. Final scope can depend on exact models, modules, bands, components, claims, HS codes, import structure, installation site, and current authority interpretation.
- Is this the same as medical device classification in Cambodia?
- No. Risk classification determines the main medical-device pathway. This checker runs after classification and looks for additional product certificates, dossier evidence, import documents, and facility or operator licences.
- Does “no separate certificate” mean no testing is required?
- No. Safety, EMC, performance, or other evidence can still be required inside the medical-device dossier even when there is no separate national product certificate.
- Is the result an official regulatory determination?
- No. It is a preliminary applicability assessment. Review the linked official source and confirm the final route with the relevant authority, certification body, importer, or regulatory professional.
DJ Fang
MedTech Regulatory Expert
Need help confirming a classification or planning your registration?
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