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Chemo Vent

FDA UDI

Class II (US FDA UDI)

by International Medical Industries Inc.

Identity

Trade Name
Chemo Vent FDA UDI
Generic Name
Hydrophobic Luer filter FDA UDI
Device Name
Venting Needle Filtered (Red) with 0.2 micron hydrophobic filter, 20 gauge x 1.5" stainless steel non-coring needle, packaged sterile, individual blister packs, 100 units per box FDA UDI
Model / Reference
31-50 FDA UDI
Description
Venting Needle Filtered (Red) with 0.2 micron hydrophobic filter, 20 gauge x 1.5" stainless steel non-coring needle, packaged sterile, individual blister packs, 100 units per box FDA UDI

Identifiers

Catalog Number
31-50 FDA UDI
Primary DI / UDI-DI
B21231501 FDA UDI
FDA Product Code
LHI FDA UDI
GMDN Term
Hydrophobic Luer filter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Category: Hydrophobic Luer filter

Chemo Vent by International Medical Industries Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hydrophobic Luer filter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c7b9ba3a-05c1-4070-a683-a765b79acc7d 34 fields · synced Jun 6, 2026