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Bosma Enterprises

FDA UDI

Class I (US FDA UDI)

by Bosma Enterprises

Identity

Trade Name
Bosma Enterprises FDA UDI
Generic Name
Surgical linen/cushion set FDA UDI
Device Name
Accelerate-OR PA Kit; Each Kit Includes QuickSuite Kit and Patient Strap. FDA UDI
Model / Reference
10-8020PA FDA UDI
Description
Accelerate-OR PA Kit; Each Kit Includes QuickSuite Kit and Patient Strap. FDA UDI

Identifiers

Catalog Number
10-8020PA FDA UDI
Primary DI / UDI-DI
00818634020611 FDA UDI
FDA Product Code
PWU FDA UDI
GMDN Term
Surgical linen/cushion set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6890 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Limb/torso/head restraint, single-useSurgical linen/cushion set

Bosma Enterprises by Bosma Enterprises — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical linen/cushion set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bosma Enterprises

Sources (1)

  • FDA UDI 5ee4c739-938c-4460-8b3c-061df7d28aaa 36 fields · synced Jun 1, 2026