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Nose It All

FDA UDI

Class I (US FDA UDI)

by Product Motif Inc.

Identity

Trade Name
Nose It All FDA UDI
Generic Name
Intranasal splint, non-biodegradable FDA UDI
Device Name
Single Pack Nosebleed Tourniquet Device - Small FDA UDI
Model / Reference
01-PN-014 FDA UDI
Description
Single Pack Nosebleed Tourniquet Device - Small FDA UDI

Identifiers

Catalog Number
01-PN-014 FDA UDI
Primary DI / UDI-DI
00860006794705 FDA UDI
FDA Product Code
EMX FDA UDI
GMDN Term
Intranasal splint, non-biodegradable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4100 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

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: Intranasal splint, non-biodegradable

Nose It All by Product Motif Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intranasal splint, non-biodegradable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Product Motif Inc.

Sources (1)

  • FDA UDI 84cae411-4473-42f0-82cf-d408398cf67f 34 fields · synced May 31, 2026