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PediTurn

EUDAMEDFDA UDI

Class I (EU MDR)

Ref IM99836GTModel Transfer Sitting

by Etac Immedia A/S

Identity

Trade Name
PediTurn EUDAMED
Immedia FDA UDI
Generic Name
Patient position turntable FDA UDI
Device Name
PediTurn EUDAMED
Model / Reference
Transfer Sitting EUDAMED
IM99836GT EUDAMED
PediTurn Soft FDA UDI

Identifiers

Catalog Number
IM99836GT FDA UDI
Primary DI / UDI-DI
05708012169702 EUDAMEDFDA UDI
Basic UDI-DI
57080123001LY EUDAMED
FDA Product Code
IKX FDA UDI
EMDN Code
Y122799 NON-MOTORIZED VEHICLES AND MEANS OF TRANSPORT - OTHER EUDAMED
GMDN Term
Patient position turntable 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

PediTurn 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 03d1ee1b-f67f-4283-9a81-80535d0bd2ab 61 fields · synced Jun 19, 2026
  • FDA UDI de63a772-463d-4f8d-915b-8e3cd0e5a6f1 33 fields · synced May 30, 2026