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BoneFoam

FDA UDI

Class I (US FDA UDI)

by Bone Foam, Inc.

Identity

Trade Name
BoneFoam FDA UDI
Generic Name
Medical equipment/instrument drape, single-use FDA UDI
Device Name
Troop | Elevation System - Disposable | Box of 3 FDA UDI
Model / Reference
10-910-00 FDA UDI
Description
Troop | Elevation System - Disposable | Box of 3 FDA UDI

Identifiers

Catalog Number
10-910-00 FDA UDI
Primary DI / UDI-DI
00810075280005 FDA UDI
FDA Product Code
CCX FDA UDI
PUI FDA UDI
GMDN Term
Medical equipment/instrument drape, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6820 FDA UDI
878.4370 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Category: Medical equipment/instrument drape, single-useOperating table patient positioning set, single-use

BoneFoam by Bone Foam, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Operating table patient positioning set, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bone Foam, Inc.

Sources (1)

  • FDA UDI 39e7add8-ae20-4660-847d-76299a609ff2 34 fields · synced May 30, 2026