Identity
- Trade Name
- Spine Instruments FDA UDI
- Generic Name
- Bone tap, single-use FDA UDI
- Device Name
- MUST MC Modular Tap 4Lead Ø4.5x30 Sterile 2X FDA UDI
- Model / Reference
- 03.51.10.7108 FDA UDI
- Description
- MUST MC Modular Tap 4Lead Ø4.5x30 Sterile 2X FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07630345732569 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Bone tap, single-use 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
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
Category: Bone tap, single-use
Spine Instruments by Medacta International — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bone tap, single-use.
- EVOS — Smith & Nephew, Inc. · Class II
- CODA™ Anterior Cervical Plate System — Pioneer Surgical Technology, Inc. · Class I
- Flower Orthopedics — FLOWER ORTHOPEDICS CORPORATION · Class I
- DELTA — Stryker Leibinger · Class II
- DELTA — Stryker Leibinger · Class II
- Nobel Biocare® — Nobel Biocare AG · Class I
- Asnis — Stryker Corp. · Class I
- NobelActive® — Nobel Biocare AG · 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
- Medacta International
Sources (1)
- FDA UDI e9101c9a-d6fa-4ef2-abe6-7bbf5c8eaefe 33 fields · synced Jun 8, 2026