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A Plus

FDA UDI

Class I (US FDA UDI)

by A Plus International, Inc

Identity

Trade Name
A Plus FDA UDI
Generic Name
Medical equipment/instrument drape, single-use FDA UDI
Device Name
Back table cover 60"x60";2.25mil ,90/BG,1350/CS FDA UDI
Model / Reference
1 FDA UDI
Description
Back table cover 60"x60";2.25mil ,90/BG,1350/CS FDA UDI

Identifiers

Catalog Number
BW60060-1 FDA UDI
Primary DI / UDI-DI
00683534210345 FDA UDI
FDA Product Code
FWZ FDA UDI
GMDN Term
Medical equipment/instrument drape, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4950 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Medical equipment/instrument drape, single-use

A Plus by A Plus International, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical equipment/instrument drape, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2fce073f-5a82-4f1d-b3d0-dd32c8f4f233 34 fields · synced Jun 1, 2026