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MANI FLEXILE FILES - 21mm #35
EUDAMEDFDA UDIClass I (EU MDR)
Ref -Model HAND FILES
by Mani, Inc.
Identity
- Trade Name
- MANI FLEXILE FILES - 21mm #35 EUDAMEDMANI FLEXILE FILES FDA UDI
- Generic Name
- Manual endodontic file/rasp, reusable FDA UDI
- Device Name
- MANI K-FILES EUDAMEDFDA UDI
- Model / Reference
- HAND FILES EUDAMED- EUDAMED21mm #35 FDA UDI
- Description
- MANI K-FILES FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04546951503888 EUDAMEDFDA UDI
- Basic UDI-DI
- 4546951000001Z9 EUDAMEDB-04546951503888 EUDAMED
- Unit of Use DI
- 74546951503887 EUDAMED
- FDA Product Code
- EKS FDA UDI
- EMDN Code
- L159004 ENDODONTIC RASPS AND FILES, REUSABLE EUDAMED
- GMDN Term
- Manual endodontic file/rasp, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 872.4565 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
CMR Substance
Yes
EUDAMEDEUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
MANI FLEXILE FILES - 21mm #35 by Mani, Inc. — Class I — MDD, MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | 4546951000001Z9 | Class I | Active |
| EUDAMED | European Union | CE/MDR | 4546951000001Z9 | Class I | Active |
| 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
- Mani, Inc.
- EUDAMED SRN
- JP-MF-000017860
- Authorised Representative
- Obelis s.a. BE-AR-000000106
Sources (3)
- EUDAMED 754e329b-39d5-4b64-9ef3-eb7a6bd3246c 61 fields · synced Jul 21, 2026
- EUDAMED 8a8db029-b645-4b60-bf4c-79aefc80f6da 61 fields · synced May 17, 2026
- FDA UDI abd25df1-035f-4230-a181-ca6bf1cc4290 33 fields · synced May 30, 2026