TMSi

FDA UDI

Class II (US FDA UDI)

by TMSi

Identity

Trade Name: TMSi FDA UDI
Generic Name: Multiple physiological signal amplifier FDA UDI
Device Name: Physiologic data acquisition device FDA UDI
Model / Reference: 8 FDA UDI
Description: Physiologic data acquisition device FDA UDI

Identifiers

Primary DI / UDI-DI: 08719481170028 FDA UDI
510(k) Number: K060374 FDA UDI
FDA Product Code: GWL FDA UDI
GMDN Term: Multiple physiological signal amplifier FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 882.1835 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Multiple physiological signal amplifier

TMSi by TMSi — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: TMSi

Sources (1)

FDA UDI 70771747-92c3-4c42-a066-6df7b65c5b07 35 fields · synced Jun 6, 2026