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ViaMed

FDA UDI

Class II (US FDA UDI)

by Rece International Corp.

Identity

Trade Name
ViaMed FDA UDI
Generic Name
Continuous electronic patient thermometer, line-powered FDA UDI
Device Name
High accuracy and fast response, easy to read digital display. Peak-hold and auto shut-off functions. Break-resistant and child-safe probe. Low battery indication. FDA UDI
Model / Reference
13110 FDA UDI
Description
High accuracy and fast response, easy to read digital display. Peak-hold and auto shut-off functions. Break-resistant and child-safe probe. Low battery indication. FDA UDI

Identifiers

Primary DI / UDI-DI
00811382015601 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
Continuous electronic patient thermometer, line-powered 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

Yes

FDA UDI

Category: Continuous electronic patient thermometer, line-powered

ViaMed by Rece International Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Continuous electronic patient thermometer, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Rece International Corp.

Sources (1)

  • FDA UDI c706fed9-2792-47d4-9d11-935fac22da5e 34 fields · synced May 31, 2026