← Back to catalogue

Fabco

FDA UDI

Class I (US FDA UDI)

by First Aid Bandage Co Inc

Identity

Trade Name
FABCO FDA UDI
Generic Name
Ear wick, non-biodegradable FDA UDI
Device Name
Ear Wick FDA UDI
Model / Reference
Q605201 FDA UDI
Description
Ear Wick FDA UDI

Identifiers

Catalog Number
Q605201 FDA UDI
Primary DI / UDI-DI
30634303800374 FDA UDI
FDA Product Code
KCN FDA UDI
GMDN Term
Ear wick, non-biodegradable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.5220 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 — 15 Millimeter FDA UDI
Outer Diameter — 9 Millimeter FDA UDI

Category: Ear wick, 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 Ear wick, non-biodegradable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 15597d72-49d9-4d4a-90e8-3133a9f9873b 36 fields · synced May 31, 2026