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Hippy | Lower Extremity Package

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 925.HIPPY-LEP

by Bone Foam, Inc.

Identity

Trade Name
Hippy | Lower Extremity Package EUDAMED
BoneFoam FDA UDI
Generic Name
Operating table patient positioning set, reusable FDA UDI
Device Name
Hippy | Lower Extremity Package EUDAMEDFDA UDI
Model / Reference
925.HIPPY-LEP EUDAMEDFDA UDI
Description
Hippy | Lower Extremity Package FDA UDI

Identifiers

Catalog Number
925.HIPPY-LEP FDA UDI
Primary DI / UDI-DI
00810075280913 EUDAMEDFDA UDI
Basic UDI-DI
081007528925HIPPYLEP6S EUDAMED
Direct Marketing DI
00810075280913 EUDAMED
FDA Product Code
CCX FDA UDI
EMDN Code
V080302 PATIENT POSITIONING MEDICAL CUSHIONS EUDAMED
GMDN Term
Operating table patient positioning set, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
868.6820 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

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

Yes

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

Hippy | Lower Extremity Package by Bone Foam, Inc. — 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
Bone Foam, Inc.
EUDAMED SRN
US-MF-000035043
Authorised Representative
Bone Foam B.V. NL-AR-000035735

Sources (2)

  • EUDAMED 6e1615a1-8c30-4a35-be96-8c1b3b7da549 61 fields · synced Jul 16, 2026
  • FDA UDI 48e56e81-561b-489f-a092-efab946b6bbd 34 fields · synced May 29, 2026