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3B-Board

EUDAMEDFDA UDI

Class I (EU MDR)

Ref IM403Model Transfer Sitting

by Etac Immedia A/S

Identity

Trade Name
3B-Board EUDAMED
Immedia FDA UDI
Generic Name
Patient transfer sliding board FDA UDI
Device Name
3B-Board EUDAMED
Model / Reference
Transfer Sitting EUDAMED
IM403 EUDAMED
3B-Board FDA UDI

Identifiers

Catalog Number
IM403 FDA UDI
Primary DI / UDI-DI
05708012451180 EUDAMEDFDA UDI
Basic UDI-DI
57080123002M2 EUDAMED
FDA Product Code
IKX FDA UDI
EMDN Code
Y122799 NON-MOTORIZED VEHICLES AND MEANS OF TRANSPORT - OTHER EUDAMED
GMDN Term
Patient transfer sliding board FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
890.5050 FDA UDI
Market of Registration
Denmark 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

3B-Board by Etac Immedia A/S — 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

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Manufacturer

Manufacturer
Etac Immedia A/S
EUDAMED SRN
DK-MF-000019241

Sources (2)

  • EUDAMED 6d4f06f1-1dc8-4ce3-8243-a77bc7ae22ed 61 fields · synced Jun 19, 2026
  • FDA UDI 6f369589-5cc6-46e9-b73d-bb0da6e9c001 33 fields · synced May 30, 2026