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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Automatic-inflation electronic sphygmomanometer, portable, finger FDA UDI
Device Name
DBD-MONITOR, BP, SPO2, EAR TEMP, PRINTER FDA UDI
Model / Reference
MDSVSMSNTTP FDA UDI
Description
DBD-MONITOR, BP, SPO2, EAR TEMP, PRINTER FDA UDI

Identifiers

Catalog Number
MDSVSMSNTTP FDA UDI
Primary DI / UDI-DI
10193489012972 FDA UDI
FDA Product Code
DQA FDA UDI
FLL FDA UDI
DXN FDA UDI
GMDN Term
Automatic-inflation electronic sphygmomanometer, portable, finger FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2700 FDA UDI
880.2910 FDA UDI
870.1130 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Automatic-inflation electronic sphygmomanometer, portable, finger

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

Similar devices

Also classified as Automatic-inflation electronic sphygmomanometer, portable, finger.

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 df4c8a52-0df1-422d-a501-e8866e731f2c 35 fields · synced Jun 1, 2026