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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Vacuum suction regulator/regulation set, general-purpose FDA UDI
Device Name
OXIMETER,PULSE,FINGER,BLUETOOTH WITH APP FDA UDI
Model / Reference
HCSM70T FDA UDI
Description
OXIMETER,PULSE,FINGER,BLUETOOTH WITH APP FDA UDI

Identifiers

Catalog Number
HCSM70T FDA UDI
Primary DI / UDI-DI
00193489094261 FDA UDI
FDA Product Code
OCH FDA UDI
GMDN Term
Vacuum suction regulator/regulation set, general-purpose FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2700 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Vacuum suction regulator/regulation set, general-purpose

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

Similar devices

Also classified as Vacuum suction regulator/regulation set, general-purpose.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI 026363d6-9927-4c91-bab4-12ecb4e90d96 36 fields · synced May 30, 2026