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Single Patient Use HoverMatt

EUDAMEDFDA UDI

Class I (EU MDR)

Ref HM34SPU-HLF-BModel Lateral Transfer Device

by HoverTech International

Identity

Trade Name
Single Patient Use HoverMatt EUDAMEDFDA UDI
Generic Name
Patient transfer system, powered FDA UDI
Device Name
34" Single Patient Use HoverMatt Half Matt Breathable FDA UDI
Model / Reference
Lateral Transfer Device EUDAMED
HM34SPU-HLF-B EUDAMEDFDA UDI
Description
34" Single Patient Use HoverMatt Half Matt Breathable FDA UDI

Identifiers

Catalog Number
HM34SPU-HLF-B FDA UDI
Primary DI / UDI-DI
00816299011081 EUDAMEDFDA UDI
Basic UDI-DI
081629901HMSM EUDAMED
FDA Product Code
FRZ FDA UDI
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
GMDN Term
Patient transfer system, powered FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
880.6775 FDA UDI
Market of Registration
Sweden 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

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Width — 34 Inch FDA UDI

Category: Device sterilization/disinfection container, reusable

Discover the Single Patient Use HoverMatt, a cutting-edge device designed for safe and effective treatment of endocrine disorders. With its simple, single-use design, this medical device is ideal for professionals in the field.

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
US-MF-000008435
Authorised Representative
Etac Supply Center AB SE-AR-000001601

Sources (2)

  • EUDAMED fae06683-0862-4b06-a01b-9f4065dc4967 61 fields · synced Jul 14, 2026
  • FDA UDI 6a399819-8192-4f86-b9f6-9cb031a268e8 37 fields · synced May 29, 2026