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Wap

FDA UDI

Class I (US FDA UDI)

by Shenzhen WAP-health Technology Co.Ltd

Identity

Trade Name
WAP FDA UDI
Generic Name
First aid kit, medicated FDA UDI
Model / Reference
1 FDA UDI

Identifiers

Primary DI / UDI-DI
06975033060069 FDA UDI
FDA Product Code
OVR FDA UDI
GMDN Term
First aid kit, medicated FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4014 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: First aid kit, medicated

Wap by Shenzhen WAP-health Technology Co.Ltd — Class I — 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

Sources (1)

  • FDA UDI bb3c7d0f-7c9b-44c9-aee4-51389d42c0c6 32 fields · synced Jun 9, 2026