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Nar

FDA UDI

Class I (US FDA UDI)

by North American Rescue, Llc.

Identity

Trade Name
NAR FDA UDI
Generic Name
Synthetic polymer burn dressing, non-coated FDA UDI
Device Name
CRAVAT - SUPER XL - DRY STERILE BURN DRESSING FDA UDI
Model / Reference
30-0162 FDA UDI
Description
CRAVAT - SUPER XL - DRY STERILE BURN DRESSING FDA UDI

Identifiers

Catalog Number
30-0162 FDA UDI
Primary DI / UDI-DI
00842209109043 FDA UDI
FDA Product Code
FPY FDA UDI
GMDN Term
Synthetic polymer burn dressing, non-coated FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5180 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Synthetic polymer burn dressing, non-coated

Nar by North American Rescue, Llc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 40c54b79-9e33-400c-b407-2a2b88a2e698 34 fields · synced May 30, 2026