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Exa Special RA - gelb

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 0733RA-25Model 16412Ref 0738RA-12Ref 0732RA-25Ref 0735RA-25

by Edenta Etablissement

Identity

Trade Name
Exa Special RA - gelb EUDAMED
EDENTA FDA UDI
Generic Name
Dental abrasive point, reusable FDA UDI
Device Name
Polierer / Arkansas EUDAMED
Exa Special RA - yellow FDA UDI
Model / Reference
16412 EUDAMED
0733RA-25 EUDAMED
0738RA-12 EUDAMEDFDA UDI
0732RA-25 EUDAMED
0735RA-25 EUDAMED
Description
Exa Special RA - yellow FDA UDI

Identifiers

Primary DI / UDI-DI
E3120733RA251 EUDAMED
E3120738RA121 EUDAMEDFDA UDI
E3120732RA251 EUDAMED
E3120735RA251 EUDAMED
Basic UDI-DI
++E31216412DU EUDAMED
Unit of Use DI
E3120738RA12101 EUDAMED
E3120732RA25101 EUDAMED
E3120733RA25101 EUDAMED
E3120735RA25101 EUDAMED
FDA Product Code
EJQ FDA UDI
EMDN Code
Q01010403 DENTAL ABRASIVE AND POLISHING MATERIALS EUDAMED
GMDN Term
Dental abrasive point, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
872.6010 FDA UDI
Market of Registration
Liechtenstein EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

A comprehensive medical device directory listing the Exa Special RA - gelb, a Class IIa device for [MEDICAL_PURPOSE]. This device is processed in a sterilization process and has been tested according to [REPROCESSED] procedures.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
LI-MF-000011937

Sources (8)

  • EUDAMED 1ff82ea5-44ec-497b-b39c-5627fb65c5a1 61 fields · synced Sep 18, 2026
  • EUDAMED d1a93f1f-ac0e-4d5b-955b-355f0cfb0936 61 fields · synced May 18, 2026
  • EUDAMED 94df701c-dd3a-4dc1-90da-958d6ea40608 61 fields · synced May 18, 2026
  • EUDAMED b655481c-8af2-49d9-b0c1-5723d9cb3dfb 61 fields · synced May 19, 2026
  • FDA UDI 637e96c3-e61a-44d9-a204-c8a499b4e530 33 fields · synced May 30, 2026
  • EUDAMED fe5db30d-1770-4107-bf0e-79ed1f77913b 61 fields · synced Jul 10, 2026
  • EUDAMED f47d2fec-378b-49d1-b10d-637bcd244ecc 61 fields · synced Jul 16, 2026
  • EUDAMED 3eda264e-b8b3-450f-974a-c6ab08ce7c4c 61 fields · synced Aug 1, 2026