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Sling

EUDAMEDFDA UDI

Class I (EU MDR)

Ref IM428Model Support

by Etac Immedia A/S

Identity

Trade Name
Sling EUDAMED
Immedia FDA UDI
Generic Name
Manual patient lifting belt/harness FDA UDI
Device Name
Sling EUDAMED
Model / Reference
Support EUDAMED
IM428 EUDAMED
Sling - long FDA UDI

Identifiers

Catalog Number
IM428 FDA UDI
Primary DI / UDI-DI
05708012206551 EUDAMEDFDA UDI
Basic UDI-DI
57080125001ME EUDAMED
FDA Product Code
IKX FDA UDI
EMDN Code
Y1299 PERSONAL MOBILITY DEVICES - OTHER EUDAMED
GMDN Term
Manual patient lifting belt/harness 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

Sling 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 a36fc407-c764-4ba7-82bf-ea3acbebe2dd 61 fields · synced Aug 3, 2026
  • FDA UDI 0e46c380-1b99-42a8-887f-0524f303c577 33 fields · synced May 30, 2026