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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
ENT diagnostic set FDA UDI
Model / Reference
20-0101 FDA UDI

Identifiers

Catalog Number
20-0101 FDA UDI
Primary DI / UDI-DI
00842209131471 FDA UDI
FDA Product Code
JYG FDA UDI
GMDN Term
ENT diagnostic set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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

Yes

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: ENT diagnostic set

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

Similar devices

Also classified as ENT diagnostic set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1730581d-6223-4219-a510-decf50d38c83 33 fields · synced May 30, 2026