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Vega

FDA UDI

Class II (US FDA UDI)

by Vega Technologies Inc.

Identity

Trade Name
VEGA FDA UDI
Generic Name
Intermittent electronic patient thermometer FDA UDI
Device Name
MT-218 FDA UDI
Model / Reference
MT-218 FDA UDI
Description
MT-218 FDA UDI

Identifiers

Primary DI / UDI-DI
06946159505024 FDA UDI
510(k) Number
K041516 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
Intermittent electronic patient thermometer 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: Intermittent electronic patient thermometer

Vega by Vega Technologies Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intermittent electronic patient thermometer.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 51c448f6-a272-437a-b551-0995c31e800d 34 fields · synced Jun 6, 2026