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Zephyr Patient Positioning and Transfer System

EUDAMEDFDA UDI

Class I (EU MDR)

Ref ZEP-AFR-01

by Diacor Inc.

Identity

Trade Name
Zephyr Patient Positioning and Transfer System EUDAMEDFDA UDI
Generic Name
Patient lifting system stretcher FDA UDI
Device Name
Zephyr Hoverboards & Accessories EUDAMED
Zephyr HDR Accessory: Footrest FDA UDI
Model / Reference
ZEP-AFR-01 EUDAMEDFDA UDI
Description
Zephyr HDR Accessory: Footrest FDA UDI

Identifiers

Primary DI / UDI-DI
B237ZEPAFR010 EUDAMEDFDA UDI
Basic UDI-DI
++B237HOVERBOARDV7 EUDAMED
510(k) Number
K121929 FDA UDI
FDA Product Code
FRZ 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
880.6775 FDA UDI
Market of Registration
Germany 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

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Patient lifting system stretcher

Zephyr Patient Positioning and Transfer System by Diacor Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient lifting system stretcher.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Diacor Inc.
EUDAMED SRN
US-MF-000017181
Authorised Representative
E C REP LIMITED IE-AR-000003995

Sources (2)

  • EUDAMED c8b51780-95c1-4b30-b7ee-66202eaedf8a 61 fields · synced Jun 1, 2026
  • FDA UDI e88d2e8b-290a-4648-a847-f33e11663081 34 fields · synced May 30, 2026