← Back to catalogue

NexTemp

FDA UDI

Class I (US FDA UDI)

by Medical Indicators

Identity

Trade Name
NexTemp FDA UDI
Generic Name
Liquid-crystal patient thermometer, reusable FDA UDI
Device Name
NexTemp Ultra Pro F Bulk Pack Clinical Thermometer FDA UDI
Model / Reference
95-2402 FDA UDI
Description
NexTemp Ultra Pro F Bulk Pack Clinical Thermometer FDA UDI

Identifiers

Catalog Number
NXT Pro F FDA UDI
Primary DI / UDI-DI
20016944401425 FDA UDI
FDA Product Code
FQZ FDA UDI
GMDN Term
Liquid-crystal patient thermometer, reusable 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

No

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 — 0.35 Gram FDA UDI

Category: Liquid-crystal patient thermometer, reusable

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, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Medical Indicators

Sources (1)

  • FDA UDI be07f6fb-49aa-4c2e-ac61-ce960cff6259 37 fields · synced Jun 6, 2026