← Back to catalogue

MANI PEESO REAMERS - 32mm #6

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref -Model Peeso Gates

by Mani, Inc.

Identity

Trade Name
MANI PEESO REAMERS - 32mm #6 EUDAMED
MANI PEESO REAMERS FDA UDI
Generic Name
Rotary/reciprocating endodontic file/rasp, reusable FDA UDI
Device Name
MANI PEESO REAMERS EUDAMEDFDA UDI
Model / Reference
- EUDAMED
Peeso Gates EUDAMED
32mm #6 FDA UDI
Description
MANI PEESO REAMERS FDA UDI

Identifiers

Primary DI / UDI-DI
04546951513115 EUDAMEDFDA UDI
Basic UDI-DI
B-04546951513115 EUDAMED
4546951000016ZN EUDAMED
Unit of Use DI
74546951513114 EUDAMED
FDA Product Code
DZA 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
872.4130 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 PEESO REAMERS - 32mm #6 by Mani, Inc. — Class IIa — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (3)

  • EUDAMED 2c49a0a2-6b71-457e-993b-4e93c63f8277 61 fields · synced Jul 28, 2026
  • EUDAMED 9b3c4bac-90a2-4feb-be78-314463e3d613 61 fields · synced May 18, 2026
  • FDA UDI 822eb8f0-88cd-4a80-adab-2dc160b4aa93 33 fields · synced May 30, 2026