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Leg Cradle

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 925.LC

by Bone Foam, Inc.

Identity

Trade Name
Leg Cradle EUDAMED
BoneFoam FDA UDI
Generic Name
Freestanding patient positioner, reusable FDA UDI
Device Name
Leg Cradle EUDAMEDFDA UDI
Model / Reference
925.LC EUDAMEDFDA UDI
Description
Leg Cradle FDA UDI

Identifiers

Catalog Number
925.LC FDA UDI
Primary DI / UDI-DI
00810075280517 EUDAMEDFDA UDI
Basic UDI-DI
081007528925LCL9 EUDAMED
Direct Marketing DI
00810075280517 EUDAMED
FDA Product Code
CCX FDA UDI
EMDN Code
V080302 PATIENT POSITIONING MEDICAL CUSHIONS EUDAMED
GMDN Term
Freestanding patient positioner, 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

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

Leg Cradle 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 c70e44a3-2fdd-4fba-80bf-51e8359f81f6 61 fields · synced Jul 25, 2026
  • FDA UDI 72803052-0f1d-4ae0-ab12-060b271604f3 34 fields · synced May 27, 2026