Identity
- Trade Name
- LIGAFIX FDA UDI
- Generic Name
- Tendon stripper FDA UDI
- Device Name
- LIGAFIX SBM closed stripper, to be used with LIGAFIX interference screws for ACL reconstruction. FDA UDI
- Model / Reference
- SBM closed stripper FDA UDI
- Description
- LIGAFIX SBM closed stripper, to be used with LIGAFIX interference screws for ACL reconstruction. FDA UDI
Identifiers
- Catalog Number
- LIG90FSTRI FDA UDI
- Primary DI / UDI-DI
- 03760154006064 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Tendon stripper 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: Tendon stripper
Ligafix by S.b.m — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Tendon stripper.
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- BOSS Instruments — Boss Instruments, Ltd. · Class I
- BOSS Instruments — Boss Instruments, Ltd. · Class I
- Surgical Direct — SURGICAL DIRECT, INC. · Class I
- Surgical Direct — SURGICAL DIRECT, INC. · Class I
- Ambler Surgical — Ambler Surgical, LLC · 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
- S.b.m
Sources (1)
- FDA UDI 198d0f46-7d4f-4d3b-af96-0f0a901194fd 34 fields · synced Jun 6, 2026