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Trinity Medical Devices

FDA UDI

Class I (US FDA UDI)

by Trinity Medical Devices Inc.

Identity

Trade Name
Trinity Medical Devices FDA UDI
Generic Name
Infant heat shield FDA UDI
Device Name
NeoGuardMiniReflectors,1inx7/8in FDA UDI
Model / Reference
4220 FDA UDI
Description
NeoGuardMiniReflectors,1inx7/8in FDA UDI

Identifiers

Primary DI / UDI-DI
00813880023133 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Infant heat shield FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5240 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

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Infant heat shield

Trinity Medical Devices by Trinity Medical Devices Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Infant heat shield.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c40e0032-5d58-4ec4-8e21-6180700a049e 33 fields · synced Jun 8, 2026