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Fabco

FDA UDI

Class I (US FDA UDI)

by First Aid Bandage Co Inc

Identity

Trade Name
FABCO FDA UDI
Generic Name
Intranasal splint, non-biodegradable FDA UDI
Device Name
Thinpack Anatomical Nasal Packing with string FDA UDI
Model / Reference
Q770411 FDA UDI
Description
Thinpack Anatomical Nasal Packing with string FDA UDI

Identifiers

Catalog Number
Q770411 FDA UDI
Primary DI / UDI-DI
30634303800558 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

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

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Height — 1.5 Centimeter FDA UDI
Width — 3.0 Centimeter FDA UDI
Length — 8.0 Centimeter FDA UDI

Category: Intranasal splint, non-biodegradable

Fabco by First Aid Bandage Co 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

Sources (1)

  • FDA UDI a30c6933-b7ee-407a-8bff-910feb41cd1b 36 fields · synced May 30, 2026