← Back to catalogue

CareGUARD

FDA UDI

Class II (US FDA UDI)

by Care Essentials Pty Ltd

Identity

Trade Name
CareGUARD FDA UDI
Generic Name
Sterilization packaging, single-use FDA UDI
Device Name
CareGUARD Dual Layers, 137cm x 137cm (54" x 54"), 60GSM, Blue/blue FDA UDI
Model / Reference
SW13713760-B/B FDA UDI
Description
CareGUARD Dual Layers, 137cm x 137cm (54" x 54"), 60GSM, Blue/blue FDA UDI

Identifiers

Catalog Number
SW13713760-B/B FDA UDI
Primary DI / UDI-DI
09332017001888 FDA UDI
FDA Product Code
FRG FDA UDI
GMDN Term
Sterilization packaging, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6850 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

Yes

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

Yes

FDA UDI

Category: Sterilization packaging, single-use

CareGUARD by Care Essentials Pty Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sterilization packaging, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 18b079d3-5398-4d8b-ac01-7c4afaecd78f 35 fields · synced May 30, 2026