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Witcaremed

FDA UDI

Class II (US FDA UDI)

by Shenzhen Witcaremed Medical Technology Co., Ltd

Identity

Trade Name
WITCAREMED FDA UDI
Generic Name
Therapeutic agent nebulizer, ambulatory FDA UDI
Device Name
Portable (Ultrasonic) Nebulizer FDA UDI
Model / Reference
NBM-3B FDA UDI
Description
Portable (Ultrasonic) Nebulizer FDA UDI

Identifiers

Primary DI / UDI-DI
06976824740184 FDA UDI
510(k) Number
K230379 FDA UDI
FDA Product Code
CAF FDA UDI
GMDN Term
Therapeutic agent nebulizer, ambulatory FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5630 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Therapeutic agent nebulizer, ambulatory

Witcaremed by Shenzhen Witcaremed Medical Technology Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Therapeutic agent nebulizer, ambulatory.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f337b596-9600-4550-801b-1ca57ce72f19 34 fields · synced May 30, 2026