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Lithotomy AirShuttle™

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref RT-5100-05Model Patient Transport

by Qfix

Identity

Trade Name
Lithotomy AirShuttle™ FDA UDI
Generic Name
Patient lifting system stretcher FDA UDI
Device Name
Lithotomy AirShuttle™ FDA UDI
Model / Reference
RT-5100-05 EUDAMEDFDA UDI
Patient Transport EUDAMED
Description
Lithotomy AirShuttle™ FDA UDI

Identifiers

Catalog Number
RT-5100-05 FDA UDI
Primary DI / UDI-DI
10841962111277 EUDAMEDFDA UDI
Basic UDI-DI
8419621PTTRANSPORTT7 EUDAMED
FDA Product Code
OUO FDA UDI
LNH FDA UDI
LHN FDA UDI
JAK FDA UDI
JAI FDA UDI
IYE FDA UDI
FRZ FDA UDI
KPS FDA UDI
EMDN Code
V080504 PATIENT TRANSFER BOARDS AND TABLES EUDAMED
GMDN Term
Patient lifting system stretcher FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
892.1200 FDA UDI
892.1000 FDA UDI
892.5050 FDA UDI
892.1750 FDA UDI
892.5770 FDA UDI
880.6775 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

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

Yes

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Patient lifting system stretcher

Lithotomy AirShuttle™ by Qfix — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Patient lifting system stretcher.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Qfix

Sources (2)

  • FDA UDI d43ab054-df0c-4b43-bea1-6d43abfc6f35 35 fields · synced Jun 20, 2026
  • EUDAMED f97784c4-7137-4493-8298-524a5f1704bc 61 fields · synced Jun 20, 2026