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Ribbed Cannula, 5x100mm
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref PS3567ULTModel TF1020
Identity
- Trade Name
- Ribbed Cannula, 5x100mm EUDAMEDUltimate Universal ribbed cannula FDA UDI
- Generic Name
- Laparoscopic access cannula, single-use FDA UDI
- Device Name
- PRIMARY TROCARS - ULTIMATE EUDAMEDThe Ultimate Cannula has applications in minimally invasive surgical procedures, and acts as a port of entry for endoscopic instruments. FDA UDI
- Model / Reference
- TF1020 EUDAMEDPS3567ULT EUDAMEDFDA UDI
- Description
- The Ultimate Cannula has applications in minimally invasive surgical procedures, and acts as a port of entry for endoscopic instruments. FDA UDI
Identifiers
- Catalog Number
- PS3567ULT FDA UDI
- Primary DI / UDI-DI
- 05051223004929 EUDAMEDFDA UDI
- Basic UDI-DI
- B-05051223004929 EUDAMED
- FDA Product Code
- HET FDA UDI
- EMDN Code
- K01010101 TROCAR STANDARD, SINGLE-USE EUDAMED
- GMDN Term
- Laparoscopic access cannula, single-use FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 884.1720 FDA UDI
- Market of Registration
- Northern Ireland EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Ribbed Cannula, 5x100mm by Purple Surgical Holdings Limited also known as Purple Surgical International Limited, Purple Surgical UK Limited and Purple…
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-05051223004929 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- EUDAMED SRN
- GB-MF-000012819
- Authorised Representative
- Advena Limited MT-AR-000000234
Sources (2)
- EUDAMED 02c0daaf-9066-4a76-bdf4-5d75a7382881 61 fields · synced Jun 17, 2026
- FDA UDI 9f4ac214-7e51-4f9b-ad07-55f31ffc9133 36 fields · synced May 30, 2026