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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
Operating room turnover kit FDA UDI
Device Name
Accelerate-OR HUO Kit; Each Kit Includes QuickSuite Kit, 40x40 Clear 2 mill Draw Tape Bag (4), 24x32 Clear Liner 1.0 mil 15 gal Bag, 4x60 Foam Positioning Strap, and Disposable Microfiber Mop Head. FDA UDI
Model / Reference
10-8020HUO FDA UDI
Description
Accelerate-OR HUO Kit; Each Kit Includes QuickSuite Kit, 40x40 Clear 2 mill Draw Tape Bag (4), 24x32 Clear Liner 1.0 mil 15 gal Bag, 4x60 Foam Positioning Strap, and Disposable Microfiber Mop Head. FDA UDI

Identifiers

Catalog Number
10-8020HUO FDA UDI
Primary DI / UDI-DI
00818634020482 FDA UDI
FDA Product Code
PWU FDA UDI
GMDN Term
Operating room turnover kit 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-useOperating room turnover kitSurgical linen/cushion setBucket liner

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

Similar devices

Also classified as Bucket liner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bosma Enterprises

Sources (1)

  • FDA UDI eaf9e27a-5870-4a96-a11a-df389bbc665a 36 fields · synced Jun 8, 2026