← Back to catalogue

Life Support Products

FDA UDI

Class II (US FDA UDI)

by Allied Medical LLC

Identity

Trade Name
Life Support Products FDA UDI
Generic Name
Demand valve FDA UDI
Device Name
Demand Valve, Trigge FDA UDI
Model / Reference
L034-101R FDA UDI
Description
Demand Valve, Trigge FDA UDI

Identifiers

Catalog Number
L034-101R FDA UDI
Primary DI / UDI-DI
00026072000373 FDA UDI
510(k) Number
K915564 FDA UDI
FDA Product Code
BTL FDA UDI
GMDN Term
Demand valve FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5925 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

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Demand valve

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

Similar devices

Also classified as Demand valve.

Cleared under the same submission

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

Manufacturer
Allied Medical LLC

Sources (1)

  • FDA UDI a5ca2de4-8e3a-424c-a699-1bdfbd2f81d3 35 fields · synced May 30, 2026