Identity
- Trade Name
- ZOLL DENTAL FDA UDI
- Generic Name
- Tooth extraction forceps FDA UDI
- Device Name
- #8 FDA UDI
- Model / Reference
- Z-1275 FDA UDI
- Description
- #8 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840105222835 FDA UDI
- FDA Product Code
- HTD FDA UDI
- GMDN Term
- Tooth extraction forceps FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Zoll Dental by Zoll-Dental — 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
- Zoll-Dental
Sources (1)
- FDA UDI e9c7492e-0e11-4b3a-92b8-b90c2cc979dc 35 fields · synced Jun 1, 2026