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MANI MEDIUM FLEXILE FILES - 25mm #12

EUDAMEDFDA UDI

Class I (EU MDR)

Ref -Model HAND FILES

by Mani, Inc.

Identity

Trade Name
MANI MEDIUM FLEXILE FILES - 25mm #12 EUDAMED
MANI MEDIUM FLEXILE 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 #12 FDA UDI
Description
MANI K-FILES FDA UDI

Identifiers

Primary DI / UDI-DI
04546951504069 EUDAMEDFDA UDI
Basic UDI-DI
B-04546951504069 EUDAMED
4546951000001Z9 EUDAMED
Unit of Use DI
74546951504068 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

Category: Manual endodontic file/rasp, reusable

MANI MEDIUM FLEXILE FILES - 25mm #12 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.

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 3a0de574-3bc9-450e-b049-1921980ee27d 61 fields · synced Jul 12, 2026
  • EUDAMED a1febdb3-947d-4481-bfe0-5610dbc5498a 61 fields · synced May 17, 2026
  • FDA UDI 891d5c01-31c6-4cda-80ee-58289df7d693 33 fields · synced May 30, 2026