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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE FDA UDI
Generic Name
Gas-sampling/monitoring respiratory tubing, single-use, sterile FDA UDI
Device Name
CONNECTOR,6-IN-1 Y, NS FDA UDI
Model / Reference
OR356 FDA UDI
Description
CONNECTOR,6-IN-1 Y, NS FDA UDI

Identifiers

Catalog Number
OR356 FDA UDI
Primary DI / UDI-DI
30888277367733 FDA UDI
FDA Product Code
GAZ FDA UDI
GMDN Term
Gas-sampling/monitoring respiratory tubing, single-use, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

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

No

FDA UDI

Category: Gas-sampling/monitoring respiratory tubing, single-use, sterile

Medline by Medline Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gas-sampling/monitoring respiratory tubing, single-use, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 09219cb4-beb8-4724-a8e4-6f9a5751014f 35 fields · synced Jun 8, 2026