← Back to catalogue

Exmoor

FDA UDI

Class I (US FDA UDI)

by Exmoor Plastics , Ltd.

Identity

Trade Name
EXMOOR FDA UDI
Generic Name
Cotton bud FDA UDI
Device Name
Mal Ear Mop FDA UDI
Model / Reference
E.301CM FDA UDI
Description
Mal Ear Mop FDA UDI

Identifiers

Catalog Number
E301CM FDA UDI
Primary DI / UDI-DI
05060180258740 FDA UDI
FDA Product Code
KXF FDA UDI
GMDN Term
Cotton bud FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6025 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

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

Yes

FDA UDI

Category: Cotton bud

Exmoor by Exmoor Plastics , Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cotton bud.

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 a40a0508-4b8d-49cb-96e8-4899a91edebd 36 fields · synced May 31, 2026