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EUDAMED registration 05051223006244No

Suction Connecting Tubing

Purple Surgical Holdings Limited also known as Purple Surgical International Limited, Purple Surgical UK Limited and Purple Surgical Manufacturing LimitedClass IEU EUDAMEDTrade name: Suction Connecting Tubing 1.8 m × 7 mm Female/Female/Male
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class I
CND nomenclatures code
A060102
Trade name
Suction Connecting Tubing 1.8 m × 7 mm Female/Female/Male
Implantable
No
Reusable
No
Measuring function
No
Registration information
Primary DI
05051223006244
Basic UDI
B-05051223006244
Version date
December 14, 2023
Manufacturer last update
September 07, 2021
Active status
No
Manufacturer
Country
United Kingdom (ex Northern Ireland)
Country type
NON_EU
Address
2 Chestnut Street Shenley
Email
glen.hillsley@purplesurgical.com
Authorized representative
SRN
MT-AR-000000234
Country
Malta
Address
Tower Street Swatar
Email
prrc@advena.mt
Regulatory information
Competent authority
Malta Medicines Authority
Applicable legislation
MDD (Directive 93/42/EEC on Medical Devices)
Placed on the market
Spain
Market available
Bulgaria:2021-12-21~None, France:2021-12-21~None, Germany:2021-12-21~None, Italy:2021-12-21~None, Portugal:2021-12-21~None, Spain:2021-12-21~None
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

SURGICAL DRAINAGE CONNECTION MEDICAL TUBES

About this record

Access comprehensive regulatory information for Suction Connecting Tubing in the European Union medical device market through Pure Global AI's free database. This Class I device is registered with EU EUDAMED under Primary DI 05051223006244 and manufactured by Purple Surgical Holdings Limited also known as Purple Surgical International Limited, Purple Surgical UK Limited and Purple Surgical Manufacturing Limited in United Kingdom (ex Northern Ireland).

This page provides complete registration details including trade name (Suction Connecting Tubing 1.8 m × 7 mm Female/Female/Male), manufacturer information, authorized representative details, competent authority (Malta Medicines Authority), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.