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Chemtron

FDA UDI

Class II (US FDA UDI)

by Allied Medical LLC

Identity

Trade Name
Chemtron FDA UDI
Generic Name
Nebulizing system delivery set, reusable FDA UDI
Device Name
Humidifier, Autoclavable FDA UDI
Model / Reference
222069-302 FDA UDI
Description
Humidifier, Autoclavable FDA UDI

Identifiers

Catalog Number
34-10-0001 FDA UDI
Primary DI / UDI-DI
00026072011027 FDA UDI
FDA Product Code
BTT FDA UDI
GMDN Term
Nebulizing system delivery set, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5450 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Nebulizing system delivery set, reusable

Chemtron by Allied Medical LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nebulizing system delivery set, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Allied Medical LLC

Sources (1)

  • FDA UDI 4087533b-7b5f-4526-ba5d-a8bd1d31a47c 34 fields · synced May 31, 2026