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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Disposable vacuum tubing FDA UDI
Device Name
TUBING,VACUUM,5/16"X100',W/40 MALE CONN FDA UDI
Model / Reference
OR500T FDA UDI
Description
TUBING,VACUUM,5/16"X100',W/40 MALE CONN FDA UDI

Identifiers

Catalog Number
OR500T FDA UDI
Primary DI / UDI-DI
30884389105713 FDA UDI
FDA Product Code
GAZ FDA UDI
GMDN Term
Disposable vacuum tubing 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Disposable vacuum tubing

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

Similar devices

Also classified as Disposable vacuum tubing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d382e0f8-7593-4350-a689-f1200fdf506c 35 fields · synced Jun 1, 2026