← Back to catalogue

Wellstar

FDA UDI

Class I (US FDA UDI)

by Asp Global, LLC

Identity

Trade Name
WELLSTAR FDA UDI
Generic Name
Basic manual toothbrush FDA UDI
Device Name
KIT, WELLSTAR AMENITY FDA UDI
Model / Reference
WSHKIT02 FDA UDI
Description
KIT, WELLSTAR AMENITY FDA UDI

Identifiers

Primary DI / UDI-DI
00840216108325 FDA UDI
FDA Product Code
EFW FDA UDI
GMDN Term
Basic manual toothbrush FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6855 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Basic manual toothbrush

Wellstar by Asp Global, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic manual toothbrush.

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

Manufacturer
Asp Global, LLC

Sources (1)

  • FDA UDI cb6f019f-772a-43e0-910e-1451a4a19973 33 fields · synced Jun 6, 2026