Identity
- Trade Name
- PEESO EUDAMEDFDA UDI
- Generic Name
- Endodontic enlarger, reusable FDA UDI
- Device Name
- PEESO EUDAMEDPeeso 132, 19 mm, # 2, handle GC FDA UDI
- Model / Reference
- 03.132.19.602.GC EUDAMEDFDA UDI
- Description
- Peeso 132, 19 mm, # 2, handle GC FDA UDI
Identifiers
- Catalog Number
- 03.132.19.602.GC FDA UDI
- Primary DI / UDI-DI
- 07640142421481 EUDAMEDFDA UDI
- Basic UDI-DI
- B-07640142421481 EUDAMED
- FDA Product Code
- DZA FDA UDI
- EMDN Code
- Q010199 CONSERVATIVE DENTISTRY AND ENDODONTICS DEVICES - OTHER EUDAMED
- GMDN Term
- Endodontic enlarger, reusable FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 872.4130 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
Peeso by FKG Dentaire Sàrl — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-07640142421481 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- FKG Dentaire Sàrl
- EUDAMED SRN
- CH-MF-000017925
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (2)
- EUDAMED d51d8da5-f9fc-4ee4-951c-9c4093571fa2 61 fields · synced Jun 17, 2026
- FDA UDI 8d2f81cd-e95f-4aff-a116-d21a7524c85b 34 fields · synced May 29, 2026