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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 Contrast, 137cm x 182cm (54" x 72"), 50GSM, Blue/white FDA UDI
Model / Reference
SW13718250-B/W FDA UDI
Description
CareGUARD Contrast, 137cm x 182cm (54" x 72"), 50GSM, Blue/white FDA UDI

Identifiers

Catalog Number
SW13718250-B/W FDA UDI
Primary DI / UDI-DI
09332017001994 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

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Manufacturer

Sources (1)

  • FDA UDI 5efe9c73-f1ac-48d1-b250-1ed500e2abf3 35 fields · synced May 30, 2026