← Back to catalogue

North American Health & Wellness

FDA UDI

Class I (US FDA UDI)

by Health & Life Co., Ltd.

Identity

Trade Name
North American Health & Wellness FDA UDI
Generic Name
Atomizer, non-ventilatory FDA UDI
Device Name
Atomizer FDA UDI
Model / Reference
JB8150 FDA UDI
Description
Atomizer FDA UDI

Identifiers

Primary DI / UDI-DI
04719872488507 FDA UDI
FDA Product Code
CCQ FDA UDI
GMDN Term
Atomizer, non-ventilatory FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5640 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

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Atomizer, non-ventilatory

North American Health & Wellness by Health & Life Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Atomizer, non-ventilatory.

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 accb1cc2-e324-4686-b927-36a258c37cc7 34 fields · synced May 30, 2026