Identity
- Trade Name
- Preat FDA UDI
- Generic Name
- Denture clasp mould FDA UDI
- Device Name
- Hader Bar Master Kit 2 FDA UDI
- Model / Reference
- 0101751 FDA UDI
- Description
- Hader Bar Master Kit 2 FDA UDI
Identifiers
- Catalog Number
- 0101751 FDA UDI
- Primary DI / UDI-DI
- 00842092113400 FDA UDI
- FDA Product Code
- EGG FDA UDI
- GMDN Term
- Denture clasp mould FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.3165 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Category: Denture clasp mould
Preat by PREAT Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Denture clasp mould.
- Hader Bar — PREAT Corporation · Class I
- Preci-Bar — PREAT Corporation · Class I
- Preci-Bar — PREAT Corporation · Class I
- Preci-Bar — PREAT Corporation · Class I
- Preat Implant Prosthetics — PREAT Corporation · Class I
- Precision Attachments — PREAT Corporation · Class I
- Hader — PREAT Corporation · Class I
- Preci-Bar — PREAT 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- PREAT Corporation
Sources (1)
- FDA UDI 36cf48cc-c8e9-4fc2-94d9-1f0306ab0544 35 fields · synced Jun 8, 2026