Identity
- Trade Name
- PANTA® FDA UDI
- Generic Name
- Bone holding forceps FDA UDI
- Device Name
- The threaded axis is part of the system used for the insertion of the nail and to perform compression. FDA UDI
- Model / Reference
- 519131ND FDA UDI
- Description
- The threaded axis is part of the system used for the insertion of the nail and to perform compression. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10381780053002 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Bone holding forceps 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Panta® by Newdeal Sas — 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
- Newdeal Sas
Sources (1)
- FDA UDI 7b9cf5e1-8437-4291-8f27-313fde2fc6cd 35 fields · synced May 30, 2026