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Top Quality Manufacturing Barrier Film

FDA UDI

Class II (US FDA UDI)

by Top Quality Manufacturing, Inc.

Identity

Trade Name
Top Quality Manufacturing Barrier Film FDA UDI
Generic Name
Medical equipment/instrument drape, single-use FDA UDI
Device Name
4" x 6" Perforated Blue Sheets Easy Peel Transparent Film Built-in Dispenser Resealable FDA UDI
Model / Reference
BF21BLU FDA UDI
Description
4" x 6" Perforated Blue Sheets Easy Peel Transparent Film Built-in Dispenser Resealable FDA UDI

Identifiers

Catalog Number
BF2-1BLU FDA UDI
Primary DI / UDI-DI
TQ27BF21BLU1 FDA UDI
FDA Product Code
PEM FDA UDI
GMDN Term
Medical equipment/instrument drape, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Medical equipment/instrument drape, single-use

Top Quality Manufacturing Barrier Film by Top Quality Manufacturing, Inc. — Class II — 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 6ddcef64-e8e6-49ed-bb9c-fa19855f1329 34 fields · synced Jun 8, 2026