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JIZAI - 013 04 31mm

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref -

by Mani, Inc.

Identity

Trade Name
JIZAI - 013 04 31mm EUDAMED
JIZAI FDA UDI
Generic Name
Rotary/reciprocating endodontic file/rasp, reusable FDA UDI
Device Name
MANI NiTi FILES EUDAMEDFDA UDI
Model / Reference
- EUDAMED
013 04 31mm FDA UDI
Description
MANI NiTi FILES FDA UDI

Identifiers

Primary DI / UDI-DI
04546951605483 EUDAMEDFDA UDI
Basic UDI-DI
4546951000015ZL EUDAMED
B-04546951605483 EUDAMED
Unit of Use DI
74546951605482 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

EUDAMED

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

JIZAI - 013 04 31mm by Mani, Inc. — Class IIa — 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 3b2d6119-7d65-4013-9758-d8d98021118b 61 fields · synced Aug 4, 2026
  • EUDAMED b5dad2d5-3578-4e2a-9343-b4c0be30b165 61 fields · synced May 19, 2026
  • FDA UDI 86c283c9-90ad-46a3-a37d-d027b9812479 33 fields · synced May 29, 2026