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Welly

FDA UDI

Class N (US FDA UDI)

by Welly Health Pbc

Identity

Trade Name
Welly FDA UDI
Generic Name
First aid kit, medicated FDA UDI
Device Name
First Aid On The Go FDA UDI
Model / Reference
WLY1013C FDA UDI
Description
First Aid On The Go FDA UDI

Identifiers

Primary DI / UDI-DI
00372663000315 FDA UDI
FDA Product Code
LRR FDA UDI
GMDN Term
First aid kit, medicated FDA UDI

Classification

Device Class
N 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
Sterilization Method
Ethylene Oxide FDA UDI

Category: First aid kit, medicated

Welly by Welly Health Pbc — Class N — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as First aid kit, medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Welly Health Pbc

Sources (1)

  • FDA UDI 516b0eb9-837e-40f8-8c25-6d5f74de0a71 34 fields · synced Jun 7, 2026