Saudi Arabia SFDA registration ME0000005467SFDAA00053
Cystoscope, Autoclavable
Product information
Autoclavable endoscopes used to provide a view of internal patient anatomy.
Product use
Intended for use in general urological and gynecological surgery through the minimally invasive approach, by utilizing natural orifices to access the surgical site.
Device classification
- Risk Class
- Class IIa
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ME0000005467SFDAA00053
- Authorization ID
- GHTF-2019-3440
- Status
- Active
- Expire Date
- October 01, 2020
Manufacturer
- Manufacturer Name
- Stryker Endoscopy
Model information
- Model ID(s)
- 0502-990-030
Product accessories
[]
About this record
Access comprehensive regulatory information for Cystoscope, Autoclavable in the Saudi Arabia medical device market through Pure Global AI's free database. This Class IIa device is registered with Saudi Arabia SFDA under registration number ME0000005467SFDAA00053 and manufactured by Stryker Endoscopy.
This page provides complete registration details including product category (Medical Device), manufacturer information, model details, and regulatory compliance data from the official Saudi Arabia SFDA medical device database. Pure Global AI offers free access to Saudi Arabia's complete medical device registry, helping global MedTech companies navigate SFDA regulations efficiently.
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