Identity
- Trade Name
- Garg FDA UDI
- Generic Name
- Dental/maxillofacial surgical procedure kit, non-medicated, reusable FDA UDI
- Device Name
- BONE GRAFT PACKER 2.4 / 2.7 mm (8-11-13-15-18 mm) TITANIUM FDA UDI
- Model / Reference
- G2033C FDA UDI
- Description
- BONE GRAFT PACKER 2.4 / 2.7 mm (8-11-13-15-18 mm) TITANIUM FDA UDI
Identifiers
- Catalog Number
- G2033C FDA UDI
- Primary DI / UDI-DI
- D943G2033C0 FDA UDI
- FDA Product Code
- MDM FDA UDI
- GMDN Term
- Dental/maxillofacial surgical procedure kit, non-medicated, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
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
No
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: Dressing/utility forceps, scissors-like, reusableDental/maxillofacial surgical procedure kit, non-medicated, reusable
Garg by Power Dental USA, Inc. — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Power Dental USA, Inc.
Sources (1)
- FDA UDI dd0ab27d-6a64-4caf-a6a7-22fc52681d9c 35 fields · synced Jun 8, 2026