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Allrap Protective Barriers

FDA UDI

Class I (US FDA UDI)

by Metrex Research

Identity

Trade Name
Allrap Protective Barriers FDA UDI
Generic Name
Instrument/equipment drape, single-use, non-sterile FDA UDI
Device Name
Roll of Perforated Sheets Blue Cover Film FDA UDI
Model / Reference
460BC FDA UDI
Description
Roll of Perforated Sheets Blue Cover Film FDA UDI

Identifiers

Primary DI / UDI-DI
00615375005095 FDA UDI
510(k) Number
K960352 FDA UDI
FDA Product Code
EFB FDA UDI
GMDN Term
Instrument/equipment drape, single-use, non-sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4200 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

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Instrument/equipment drape, single-use, non-sterile

Allrap Protective Barriers by Metrex Research — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument/equipment drape, single-use, non-sterile.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Metrex Research

Sources (1)

  • FDA UDI 1ae0cc1a-2066-4325-92dd-5b0d0f051f0c 36 fields · synced May 30, 2026