← Back to catalogue

Mini Mat Gray

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 20Z480IRef 50Z480I

by Zirc Dental Products Inc.

Identity

Trade Name
Mini Mat Gray EUDAMED
Mini Mat FDA UDI
Generic Name
Sterilization packaging, reusable FDA UDI
Device Name
Dental Cleaning, Sterilization, Disinfection Accessories EUDAMED
Mini Mat Gray EUDAMED
Instrument holder intended for 8 dental instruments for sterilization. FDA UDI
Model / Reference
20Z480I EUDAMED
50Z480I EUDAMED
I-Gray FDA UDI
Description
Instrument holder intended for 8 dental instruments for sterilization. FDA UDI

Identifiers

Catalog Number
50Z480I FDA UDI
Primary DI / UDI-DI
00840161301178 EUDAMED
D68550Z480I0 FDA UDI
Basic UDI-DI
0840161300083F EUDAMED
B-00840161301178 EUDAMED
FDA Product Code
FSM FDA UDI
EMDN Code
S010401 TRAYS, BASKETS, TUBS FOR STERILISATION AND THEIR COMPONENTS EUDAMED
GMDN Term
Sterilization packaging, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4800 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

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

Category: Instrument tray, reusable

Mini Mat Gray by Zirc Dental Products, Inc. — Class I — MDD, MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument tray, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

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
US-MF-000021065
Authorised Representative
Medicom GmbH DE-AR-000005612

Sources (3)

  • EUDAMED a063910e-9617-425f-bd46-39879ba3cb3b 61 fields · synced Jul 11, 2026
  • EUDAMED 4818d090-a9e4-4ba0-897d-c3575109d0d1 61 fields · synced May 17, 2026
  • FDA UDI 56c4d664-648c-4893-8d6d-36a2099d0083 34 fields · synced May 29, 2026