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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
Ophthalmic/otologic diagnostic set FDA UDI
Device Name
KIT, CORPSMAN FIELD - Basic FDA UDI
Model / Reference
20-0001 FDA UDI
Description
KIT, CORPSMAN FIELD - Basic FDA UDI

Identifiers

Catalog Number
20-0001 FDA UDI
Primary DI / UDI-DI
00842209110988 FDA UDI
FDA Product Code
OHO FDA UDI
GMDN Term
Ophthalmic/otologic diagnostic set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4014 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

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: Ophthalmic/otologic 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 Ophthalmic/otologic diagnostic set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0192f2ab-a27a-426e-bfe1-a8741e093035 34 fields · synced Jun 8, 2026