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SunTech Tango M2 Kit

FDA UDI

Class II (US FDA UDI)

by Mortara Instrument, Inc.

Identity

Trade Name
SunTech Tango M2 Kit FDA UDI
Generic Name
Automatic-inflation electronic sphygmomanometer, non-portable FDA UDI
Device Name
SUNTECH TANGO M2 BP MONITOR KIT QS V4 FDA UDI
Model / Reference
9922-020-50 FDA UDI
Description
SUNTECH TANGO M2 BP MONITOR KIT QS V4 FDA UDI

Identifiers

Primary DI / UDI-DI
00812345029772 FDA UDI
FDA Product Code
DPS FDA UDI
GMDN Term
Automatic-inflation electronic sphygmomanometer, non-portable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2340 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Automatic-inflation electronic sphygmomanometer, non-portable

SunTech Tango M2 Kit by Mortara Instrument, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5940fb7b-9a9e-40ec-85f7-aab92844db5c 35 fields · synced Jun 8, 2026