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PureLife+ CSR Wrap

FDA UDI

Class II (US FDA UDI)

by Purelife, Llc

Identity

Trade Name
PureLife+ CSR Wrap FDA UDI
Generic Name
Medical equipment/instrument drape, single-use FDA UDI
Device Name
PureLife+ CSR Wrap , 15" x 15" , Provides barrier against air and water-borne bacteria FDA UDI
Model / Reference
1192102 FDA UDI
Description
PureLife+ CSR Wrap , 15" x 15" , Provides barrier against air and water-borne bacteria FDA UDI

Identifiers

Catalog Number
1192102 FDA UDI
Primary DI / UDI-DI
D79011921021 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Medical equipment/instrument drape, single-use

PureLife+ CSR Wrap by Purelife, Llc — 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

Manufacturer
Purelife, Llc

Sources (1)

  • FDA UDI 1a1c4cac-ef48-4fad-bc5c-af2161b4cfec 35 fields · synced Jun 1, 2026