Identity
- Trade Name
- Comprehensive® Instruments FDA UDI
- Generic Name
- Cannulated surgical drill guiding pin FDA UDI
- Model / Reference
- 110003484 FDA UDI
Identifiers
- Catalog Number
- 110003484 FDA UDI
- Primary DI / UDI-DI
- 00887868462634 FDA UDI
- FDA Product Code
- HSD FDA UDIMBF FDA UDIKWS FDA UDIKWT FDA UDI
- GMDN Term
- Cannulated surgical drill guiding pin FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3690 FDA UDI888.3670 FDA UDI888.3660 FDA UDI888.3650 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Cannulated surgical drill guiding pin
Comprehensive® Instruments by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- COMPREHENSIVE INSTRUMENTS — Biomet Orthopedics, Inc.
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- COMPREHENSIVE INSTRUMENTS — Biomet Orthopedics, Inc.
- COMPREHENSIVE INSTRUMENTS — Biomet Orthopedics, Inc.
- COMPREHENSIVE INSTRUMENTS — Biomet Orthopedics, Inc.
K193038 also covers:
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- COMPREHENSIVE SHOULDER SYSTEM — Biomet Orthopedics, Inc.
- COMPREHENSIVE SHOULDER SYSTEM — Biomet Orthopedics, Inc.
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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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Biomet Orthopedics, Inc.
Sources (1)
- FDA UDI dff53034-593e-4169-bb11-ae0c840be9d2 36 fields · synced May 30, 2026