← Back to catalogue

Ventlab

FDA UDI

Class I (US FDA UDI)

by Ventlab Corp.

Identity

Trade Name
Ventlab FDA UDI
Generic Name
Heat/moisture exchanger, single-use FDA UDI
Device Name
15MM x 15MM OD CONN W/15MM 6" FLEX TUBE FDA UDI
Model / Reference
FH106347 FDA UDI
Description
15MM x 15MM OD CONN W/15MM 6" FLEX TUBE FDA UDI

Identifiers

Catalog Number
FH106347 FDA UDI
Primary DI / UDI-DI
10889483103302 FDA UDI
FDA Product Code
BYD FDA UDI
GMDN Term
Heat/moisture exchanger, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5375 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 15 Millimeter FDA UDI

Category: Heat/moisture exchanger, single-use

Ventlab by Ventlab Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Heat/moisture exchanger, single-use.

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
Ventlab Corp.

Sources (1)

  • FDA UDI c531434e-8912-4f18-9e1e-9d13b59786c6 36 fields · synced May 30, 2026