Identity
- Trade Name
- HU-FRIEDY FDA UDI
- Generic Name
- Rubber dam punch FDA UDI
- Device Name
- Rubber Dam Punch FDA UDI
- Model / Reference
- ARDP FDA UDI
- Description
- Rubber Dam Punch FDA UDI
Identifiers
- Catalog Number
- ARDP FDA UDI
- Primary DI / UDI-DI
- 10889950123789 FDA UDI
- FDA Product Code
- EJG FDA UDI
- GMDN Term
- Rubber dam punch FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.6300 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
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: Rubber dam punch
Hu-Friedy by Hu-Friedy Mfg Co., Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Rubber dam punch.
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- American Medicals — AMERICAN MEDICALS · Class I
- Pomee — POMEE CORPORATION · Class I
- HYGENIC — Coltene/Whaledent Inc. · Class I
- Pomee — POMEE CORPORATION · Class I
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
- Hu-Friedy Mfg Co., Llc
Sources (1)
- FDA UDI aeba72a1-3a6a-4f76-91d7-2241aaf40958 35 fields · synced May 31, 2026