Identity
- Trade Name
- PEESO REAMERS RA, N°5 FDA UDI
- Generic Name
- Endodontic enlarger, reusable FDA UDI
- Device Name
- Rack of 6 - 32 mm length - Diam 1.50 Peeso Reamers are mechanized dental instruments used for accessing to the root canal and enlarging the opening of the coronal part of the root canal, before and after using files. Peeso Reamers are also used for pin or post hole preparation. FDA UDI
- Model / Reference
- 20442 FDA UDI
- Description
- Rack of 6 - 32 mm length - Diam 1.50 Peeso Reamers are mechanized dental instruments used for accessing to the root canal and enlarging the opening of the coronal part of the root canal, before and after using files. Peeso Reamers are also used for pin or post hole preparation. FDA UDI
Identifiers
- Primary DI / UDI-DI
- J01020442 FDA UDI
- FDA Product Code
- DZA FDA UDI
- GMDN Term
- Endodontic enlarger, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4130 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
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
Category: Endodontic enlarger, reusable
Peeso Reamers Ra, N°5 by Produits dentaires S.A. — 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
- Produits dentaires S.A.
Sources (1)
- FDA UDI e4287eac-10fa-435b-809f-f1021de87bbc 34 fields · synced Jun 6, 2026