MANI REAMERS - 21mm #60
EUDAMEDFDA UDIClass I (EU MDR)
by Mani, Inc.
Identity
- Trade Name
- MANI REAMERS - 21mm #60 EUDAMEDMANI REAMERS FDA UDI
- Generic Name
- Manual endodontic file/rasp, reusable FDA UDI
- Device Name
- MANI REAMERS EUDAMEDFDA UDI
- Model / Reference
- HAND FILES EUDAMED- EUDAMED21mm #60 FDA UDI
- Description
- MANI REAMERS FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04546951500924 EUDAMEDFDA UDI
- Basic UDI-DI
- 4546951000001Z9 EUDAMEDB-04546951500924 EUDAMED
- Unit of Use DI
- 74546951500923 EUDAMED
- FDA Product Code
- EKP 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 REAMERS - 21mm #60 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 |
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 90d86598-8413-4960-ad9b-b31631fb39f1 61 fields · synced Jul 10, 2026
- EUDAMED 48e051ba-dda3-4a14-a64d-7d64b1724288 61 fields · synced May 18, 2026
- FDA UDI e846b02f-c7ff-429b-97d2-7d2776a5c120 33 fields · synced May 30, 2026