Identity
- Trade Name
- Speed-Lock FDA UDI
- Generic Name
- Arthroscopic access cannula, reusable FDA UDI
- Device Name
- Cannula, 1 Rotating Stopcock FDA UDI
- Model / Reference
- 0377031630 FDA UDI
- Description
- Cannula, 1 Rotating Stopcock FDA UDI
Identifiers
- Catalog Number
- 377-031-630 FDA UDI
- Primary DI / UDI-DI
- 07613327057775 FDA UDI
- FDA Product Code
- NBH FDA UDIFSM FDA UDI
- GMDN Term
- Arthroscopic access cannula, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.1100 FDA UDI878.4800 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Arthroscopic access cannula, reusable
Speed-Lock by Stryker Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Arthroscopic access cannula, reusable.
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- Arthrex® — Arthrex, Inc. · Class I
- Arthrex® — Arthrex, Inc. · Class I
- INFLOW CANNULA SET — SONTEC INSTRUMENTS, INC. · Class I
- Arthrex® — Arthrex, Inc. · Class I
- OBTURATOR — SONTEC INSTRUMENTS, 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 |
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Manufacturer
- Manufacturer
- Stryker Corp.
Sources (1)
- FDA UDI bbaa3e9a-cddd-45c3-9525-7723df23d0d6 36 fields · synced May 31, 2026