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Procure

FDA UDI

Class I (US FDA UDI)

by Twin Med, LLC

Identity

Trade Name
Procure FDA UDI
Generic Name
Therapeutic agent nebulizer, benchtop FDA UDI
Device Name
Small Volume Nebulizer Anti-Spill T Mouthpiece 6" Reservoir Tube 7' Kink Resistant Tubing W/Universal Connector FDA UDI
Model / Reference
1002349 FDA UDI
Description
Small Volume Nebulizer Anti-Spill T Mouthpiece 6" Reservoir Tube 7' Kink Resistant Tubing W/Universal Connector FDA UDI

Identifiers

Catalog Number
1002349 FDA UDI
Primary DI / UDI-DI
10840330700495 FDA UDI
FDA Product Code
CCQ FDA UDI
GMDN Term
Therapeutic agent nebulizer, benchtop 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

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Therapeutic agent nebulizer, benchtop

Procure by Twin Med, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Therapeutic agent nebulizer, benchtop.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Twin Med, LLC

Sources (1)

  • FDA UDI 9bfc20fe-59b6-49c3-9124-28d7d09c46a3 36 fields · synced May 30, 2026