Identity
- Trade Name
- Cannulated Screws FDA UDI
- Generic Name
- Surgical drill chuck FDA UDI
- Device Name
- CANNULATED CORTEX REAMER 4.0MM WMOD CHUCK FDA UDI
- Model / Reference
- 71932541 FDA UDI
- Description
- CANNULATED CORTEX REAMER 4.0MM WMOD CHUCK FDA UDI
Identifiers
- Catalog Number
- 71932541 FDA UDI
- Primary DI / UDI-DI
- 00885556145197 FDA UDI
- 510(k) Number
- K123055 FDA UDI
- FDA Product Code
- HRS FDA UDI
- GMDN Term
- Surgical drill chuck FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3030 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Surgical drill chuck
Cannulated Screws by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical drill chuck.
- De Soutter Medical — De Soutter Medical, Ltd. · Class I
- ELMED — ELMED INCORPORATED · Class I
- De Soutter Medical — De Soutter Medical, Ltd. · Class I
- De Soutter Medical — De Soutter Medical, Ltd. · Class I
- gSource — GSOURCE, LLC. · Class II
- De Soutter Medical — De Soutter Medical, Ltd. · Class I
- MicroAire® — MicroAire Surgical Instruments LLC · Class I
- AO — Stryker Corp. · Class I
Cleared under the same submission
K123055 also covers:
- BIRMINGHAM HIP RESURFACING(BHR) — Smith & Nephew, Inc.
- CHS — Smith & Nephew, Inc.
- CHS — Smith & Nephew, Inc.
- Cannulated Screws — Smith & Nephew, Inc.
- Cannulated Screws — Smith & Nephew, Inc.
- Cannulated Screws — Smith & Nephew, Inc.
- Jet-X — Smith & Nephew, Inc.
- LARGE CANNULATED SCREWS — Smith & Nephew, Inc.
- LARGE CANNULATED SCREWS — Smith & Nephew, Inc.
- LARGE CANNULATED SCREWS — Smith & Nephew, Inc.
- LEGION — Smith & Nephew, Inc.
- LEGION — Smith & Nephew, Inc.
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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Smith & Nephew, Inc.
Sources (1)
- FDA UDI 215f339d-ad97-4501-b03d-a30b2aab2e2f 36 fields · synced Jun 8, 2026