Identity
- Trade Name
- SMR Shoulder FDA UDI
- Generic Name
- Orthopaedic implant/instrument dismantling device FDA UDI
- Device Name
- Extracting Pliers for Reverse Trial Liners FDA UDI
- Model / Reference
- 9013.60.101 FDA UDI
- Description
- Extracting Pliers for Reverse Trial Liners FDA UDI
Identifiers
- Catalog Number
- 9013.60.101 FDA UDI
- Primary DI / UDI-DI
- 08033390109956 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Orthopaedic implant/instrument dismantling device FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
SMR Shoulder by Limacorporate — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Limacorporate
Sources (1)
- FDA UDI d76382fe-5010-45e8-967d-75e1718fdfe5 35 fields · synced Jun 6, 2026