Identity
- Trade Name
- DRI-LOK FDA UDI
- Generic Name
- Arthroscopic access cannula, single-use FDA UDI
- Device Name
- [Distal Threaded Cannula. Do not resterilize, Do not use if package is damaged] FDA UDI
- Model / Reference
- 3910075802 FDA UDI
- Description
- [Distal Threaded Cannula. Do not resterilize, Do not use if package is damaged] FDA UDI
Identifiers
- Catalog Number
- 3910-075-802 FDA UDI
- Primary DI / UDI-DI
- 07613327055740 FDA UDI
- FDA Product Code
- NBH FDA UDI
- GMDN Term
- Arthroscopic access cannula, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.1100 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
Dimensions & Sizes
- Size
- Outer Diameter — 8.0 Millimeter FDA UDILength — 75.0 Millimeter FDA UDI
Category: Arthroscopic access cannula, single-use
Dri-Lok by Stryker Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Arthroscopic access cannula, single-use.
- ZEOS — SANTA BARBARA IMAGING SYSTEMS, INC. · Class I
- Arthrex® — Arthrex, Inc. · Class I
- SportMed Instruments — Medacta International · Class I
- HYDRODAM™ CANNULA SYSTEM — Biomet Orthopedics, Inc. · Class I
- HYDRODAM™ CANNULA SYSTEM — Biomet Orthopedics, Inc. · Class I
- Arthrex® — Arthrex, Inc. · Class I
- HYDRODAM™ CANNULA SYSTEM — Biomet Orthopedics, Inc. · Class I
- Arthrex® — Arthrex, Inc. · Class I
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Stryker Corp.
Sources (1)
- FDA UDI 7b04d8eb-4f33-4215-8df7-702e93823579 36 fields · synced Jun 6, 2026