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Reprocessed Threaded Clear Cannula with Obturator, 5.5mm x 75mm
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- Reprocessed Threaded Clear Cannula with Obturator, 5.5mm x 75mm FDA UDI
- Generic Name
- Arthroscopic access cannula, single-use FDA UDI
- Model / Reference
- 214108 FDA UDI
Identifiers
- Primary DI / UDI-DI
- B3902141081 FDA UDI
- FDA Product Code
- GEA FDA UDI
- GMDN Term
- Arthroscopic access cannula, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Arthroscopic access cannula, single-use
Reprocessed Threaded Clear Cannula with Obturator, 5.5mm x 75mm by Suretek Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Arthroscopic access cannula, single-use.
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Suretek Medical
Sources (1)
- FDA UDI 1f3be8e1-f7f6-468d-8700-8751e2d9f6a1 32 fields · synced Jun 6, 2026