Identity
- Trade Name
- SHOULDER INNOVATIONS TSA SYSTEM FDA UDI
- Generic Name
- Device sterilization/disinfection container, reusable FDA UDI
- Device Name
- Instrument Case Base, original Shoulder Innovations case base modified to hold InSet Plus glenoid trials FDA UDI
- Model / Reference
- InSet Plus Case Base FDA UDI
- Description
- Instrument Case Base, original Shoulder Innovations case base modified to hold InSet Plus glenoid trials FDA UDI
Identifiers
- Catalog Number
- 2N1AB00003 FDA UDI
- Primary DI / UDI-DI
- B1132N1AB00003 FDA UDI
- FDA Product Code
- KWS FDA UDIKWT FDA UDIHSD FDA UDI
- GMDN Term
- Device sterilization/disinfection container, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3660 FDA UDI888.3650 FDA UDI888.3690 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
No
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
Category: Device sterilization/disinfection container, reusable
Shoulder Innovations Tsa System by SHOULDER INNOVATIONS, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 |
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Manufacturer
- Manufacturer
- SHOULDER INNOVATIONS, Inc
Sources (1)
- FDA UDI d7807ff6-fadf-4f86-977e-6eafbb2a8f1a 35 fields · synced May 30, 2026