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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Suction system filter, microbial FDA UDI
Device Name
SET, SUCTION FILTERS, TUBING FDA UDI
Model / Reference
HCS7001SET FDA UDI
Description
SET, SUCTION FILTERS, TUBING FDA UDI

Identifiers

Catalog Number
HCS7001SET FDA UDI
Primary DI / UDI-DI
00193489084613 FDA UDI
FDA Product Code
OJR FDA UDI
GMDN Term
Suction system filter, microbial FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4780 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Suction system filter, microbial

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

Similar devices

Also classified as Suction system filter, microbial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI eb6fb621-6f07-4a5d-bd74-ab0a7b067da7 36 fields · synced Jun 8, 2026