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NuvoMed

FDA UDI

Class II (US FDA UDI)

by Nuvomed Inc

Identity

Trade Name
NuvoMed FDA UDI
Generic Name
General-purpose patient temperature probe, single-use FDA UDI
Device Name
Wireless Infrared Thermometer FDA UDI
Model / Reference
NIET-6/0702 FDA UDI
Description
Wireless Infrared Thermometer FDA UDI

Identifiers

Primary DI / UDI-DI
00859811007025 FDA UDI
510(k) Number
K152640 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
General-purpose patient temperature probe, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2910 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General-purpose patient temperature probe, single-use

NuvoMed by Nuvomed Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose patient temperature probe, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nuvomed Inc

Sources (1)

  • FDA UDI 1b0c050c-5c83-4d58-94c6-074ed0bae04d 34 fields · synced May 31, 2026