Identity
- Trade Name
- 9MM PLUNGER FOR FDA UDI
- Generic Name
- Cannulated surgical drill guiding pin FDA UDI
- Model / Reference
- 900784 FDA UDI
Identifiers
- Catalog Number
- 900784 FDA UDI
- Primary DI / UDI-DI
- 00880304563247 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Cannulated surgical drill guiding pin FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Cannulated surgical drill guiding pin
9mm Plunger For by Biomet Orthopedics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cannulated surgical drill guiding pin.
- TRIGEN — Smith & Nephew, Inc. · Class II
- MEDLINE UNITE — MEDLINE INDUSTRIES, INC. · Class I
- Implant-One — Implant Logistics, Inc. · Class I
- CONQUEST FN — Smith & Nephew, Inc. · Class II
- EPIC CANNULATED SCREW SYSTEM — Exactech, Inc. · Class II
- Superhawk — RESPONSIVE ORTHOPEDICS LLC · Class I
- MEDLINE UNITE — MEDLINE INDUSTRIES, INC. · Class I
- Hyper-C — Degen Medical · 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
- Biomet Orthopedics, Inc.
Sources (1)
- FDA UDI 12933e0b-ef28-48ca-869b-16dbbd0fd497 34 fields · synced Jun 6, 2026