Identity
- Trade Name
- TSI FDA UDI
- Generic Name
- Bone lever/elevator, reusable FDA UDI
- Device Name
- LATERAL PROBE, SHORT, 150 MM FDA UDI
- Model / Reference
- ML-0336 FDA UDI
- Description
- LATERAL PROBE, SHORT, 150 MM FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00843059120752 FDA UDI
- FDA Product Code
- HXB FDA UDI
- GMDN Term
- Bone lever/elevator, reusable 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
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Tsi by Tedan Surgical Innovations, L.l.c. — 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
- Tedan Surgical Innovations, L.l.c.
Sources (1)
- FDA UDI fd760ee8-c393-43e7-bb2d-be77bd7cf7de 34 fields · synced Jun 1, 2026