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MANI K-FILES - 25mm #08

EUDAMEDFDA UDI

Class I (EU MDR)

Ref -Model HAND FILES

by Mani, Inc.

Identity

Trade Name
MANI K-FILES - 25mm #08 EUDAMED
MANI K-FILES FDA UDI
Generic Name
Manual endodontic file/rasp, reusable FDA UDI
Device Name
MANI K-FILES EUDAMEDFDA UDI
Model / Reference
- EUDAMED
HAND FILES EUDAMED
25mm #08 FDA UDI
Description
MANI K-FILES FDA UDI

Identifiers

Primary DI / UDI-DI
04546951501891 EUDAMEDFDA UDI
Basic UDI-DI
B-04546951501891 EUDAMED
4546951000001Z9 EUDAMED
Unit of Use DI
74546951501890 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

No

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

MANI K-FILES - 25mm #08 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

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Manufacturer

Manufacturer
Mani, Inc.
EUDAMED SRN
JP-MF-000017860
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (3)

  • EUDAMED 7f147ad7-ab57-4a97-a354-90e4141ce027 61 fields · synced Jul 9, 2026
  • EUDAMED 35cca923-ce30-4d6f-b62d-a6d0e97c87a8 61 fields · synced May 17, 2026
  • FDA UDI 4912a790-8b51-4c88-a00e-a27c308f8bef 33 fields · synced May 30, 2026