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MANI SUPER FILES - 21mm #15

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref -

by Mani, Inc.

Identity

Trade Name
MANI SUPER FILES - 21mm #15 EUDAMED
MANI SUPER FILES FDA UDI
Generic Name
Rotary/reciprocating endodontic file/rasp, reusable FDA UDI
Device Name
MANI SUPER FILES EUDAMEDFDA UDI
Rotary SUS Files EUDAMED
Model / Reference
- EUDAMED
21mm #15 FDA UDI
Description
MANI SUPER FILES FDA UDI

Identifiers

Primary DI / UDI-DI
04546951514532 EUDAMEDFDA UDI
Basic UDI-DI
B-04546951514532 EUDAMED
4546951000013ZG EUDAMED
Unit of Use DI
74546951514531 EUDAMED
FDA Product Code
EKS FDA UDI
EMDN Code
L159004 ENDODONTIC RASPS AND FILES, REUSABLE EUDAMED
GMDN Term
Rotary/reciprocating endodontic file/rasp, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA 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 SUPER FILES - 21mm #15 by Mani, Inc. — Class IIa — MDR, MDD, 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/MDR

European Union Active

CE/MDD

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 0c0a75a4-f45b-4541-82a1-f957d228e4f4 61 fields · synced Jul 23, 2026
  • EUDAMED d01e5d21-8e91-402d-ba87-725d015c1954 61 fields · synced May 18, 2026
  • FDA UDI cb470c20-249b-421b-818e-b87938e92f8c 33 fields · synced May 30, 2026