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NexTemp

FDA UDI

Class I (US FDA UDI)

by Medical Indicators

Identity

Trade Name
NexTemp FDA UDI
Generic Name
Liquid-crystal patient thermometer, single-use FDA UDI
Device Name
NexTemp GO F single-use clinical thermometer DTC 12pk FDA UDI
Model / Reference
8500-12 FDA UDI
Description
NexTemp GO F single-use clinical thermometer DTC 12pk FDA UDI

Identifiers

Catalog Number
NXT GO F FDA UDI
Primary DI / UDI-DI
00016944401452 FDA UDI
FDA Product Code
FQZ FDA UDI
GMDN Term
Liquid-crystal patient thermometer, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.2900 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

No

FDA UDI

Dimensions & Sizes

Size
Weight — 0.23 Gram FDA UDI

Category: Liquid-crystal patient thermometer, single-use

NexTemp by Medical Indicators — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Liquid-crystal patient thermometer, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medical Indicators

Sources (1)

  • FDA UDI 86232c24-9457-4078-8bca-5a2db5167665 37 fields · synced Jun 6, 2026