MANI H-FILES - 31mm #30
EUDAMEDFDA UDIClass I (EU MDR)
by Mani, Inc.
Identity
- Trade Name
- MANI H-FILES - 31mm #30 EUDAMEDMANI H-FILES FDA UDI
- Generic Name
- Manual endodontic file/rasp, reusable FDA UDI
- Device Name
- MANI H-FILES EUDAMEDFDA UDI
- Model / Reference
- HAND FILES EUDAMED- EUDAMED31MM #30 FDA UDI
- Description
- MANI H-FILES FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04546951503529 EUDAMEDFDA UDI
- Basic UDI-DI
- 4546951000001Z9 EUDAMEDB-04546951503529 EUDAMED
- Unit of Use DI
- 74546951503528 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
Single Use
No
Implantable
No
Reusable
Yes
Contains Latex
No
Reprocessed
No
CMR Substance
Yes
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
No
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
Yes
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
Yes
Manufacturing Date
Yes
Category: Manual endodontic file/rasp, reusable
MANI H-FILES - 31mm #30 by Mani, Inc. — Class I — MDD, MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Manual endodontic file/rasp, reusable.
- K-Files 21mm 070, pu: 6 pcs — Diaswiss SA · Class I
- REAMERS — DiaDent Group International · Class I
- K-Files — MICRO MEGA · Class I
- Hand instrument K-file — TULSA DENTAL PRODUCTS LLC · Class I
- Endodontic Files — CHANGZHOU SIFARY MEDICAL TECHNOLOGY CO., LTD. · Class IIa
- ProFile .04 Taper Hand File — TULSA DENTAL PRODUCTS LLC · Class I
- KOMET Root Canal Files — Gebr. Brasseler GmbH & Co. KG · Class I
- Endodontic Files — CHANGZHOU SIFARY MEDICAL TECHNOLOGY CO., LTD. · Class IIa
Authorization Coverage (2 countries)
Regulatory Authorizations
CE/MDD
CE/MDR
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 |
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Manufacturer
- Manufacturer
- Mani, Inc.
- EUDAMED SRN
- JP-MF-000017860
- Authorised Representative
- Obelis s.a. BE-AR-000000106
Sources (3)
- EUDAMED f7474d28-5fea-4a19-989b-788ffae3452d 61 fields · synced Aug 2, 2026
- EUDAMED 4d49601d-3b7b-4d7e-9cc8-ace1fa31a879 61 fields · synced May 18, 2026
- FDA UDI b7030e31-e141-4436-b198-3dfc43294c35 33 fields · synced May 30, 2026