← Back to catalogue

Anti-Fatigue Mats

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 810-3601

by Batrik Medical Manufacturing Inc.

Identity

Trade Name
Batrik NIMBUS Floor Mat 24"x36" Taupe FDA UDI
Generic Name
Anti-fatigue floor mat FDA UDI
Device Name
Anti-Fatigue Mats EUDAMED
Blue Cloud Nimbus Anti-Fatigue Mat, Taupe, 24" x 36" (61 cm X 91 cm) FDA UDI
Model / Reference
810-3601 EUDAMEDFDA UDI
Description
Blue Cloud Nimbus Anti-Fatigue Mat, Taupe, 24" x 36" (61 cm X 91 cm) FDA UDI

Identifiers

Catalog Number
810-3601 FDA UDI
Primary DI / UDI-DI
00690521011793 EUDAMEDFDA UDI
Basic UDI-DI
6905210ANTIFATIGMAT100EB EUDAMED
FDA Product Code
CCX FDA UDI
EMDN Code
V0899 MEDICAL SUPPORT EQUIPMENT - OTHER EUDAMED
GMDN Term
Anti-fatigue floor mat FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
868.6820 FDA UDI
Market of Registration
Ireland 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

Anti-Fatigue Mats by Batrik Medical Manufacturing Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

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
CA-MF-000007738
Authorised Representative
Advena Limited MT-AR-000000234

Sources (2)

  • EUDAMED d393e177-9dac-4a7c-b686-5437dafc624f 61 fields · synced Jul 29, 2026
  • FDA UDI 92c2bb09-223f-4733-a354-277851c674b6 36 fields · synced May 29, 2026