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JIZAI - 035 04 31mm

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref -

by Mani, Inc.

Identity

Trade Name
JIZAI - 035 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
035 04 31mm FDA UDI
Description
MANI NiTi FILES FDA UDI

Identifiers

Primary DI / UDI-DI
04546951605643 EUDAMEDFDA UDI
Basic UDI-DI
4546951000015ZL EUDAMED
B-04546951605643 EUDAMED
Unit of Use DI
74546951605642 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 - 035 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 ca83f1bf-5214-496c-bc8c-52ea366a4a24 61 fields · synced Jul 24, 2026
  • EUDAMED c42d4d98-4bbe-47fb-b3d3-3162d02d6b66 61 fields · synced May 19, 2026
  • FDA UDI b1795cdb-b2b1-4b9c-8130-da2d48f5c624 33 fields · synced May 30, 2026