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Meijer

FDA UDI

Class II (US FDA UDI)

by Meijer, Inc.

Identity

Trade Name
Meijer FDA UDI
Generic Name
Infrared patient thermometer, skin FDA UDI
Device Name
Meijer Deluxe Temple Touch Thermometer FDA UDI
Model / Reference
74-335 FDA UDI
Description
Meijer Deluxe Temple Touch Thermometer FDA UDI

Identifiers

Primary DI / UDI-DI
00713733353953 FDA UDI
510(k) Number
K032362 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
Infrared patient thermometer, skin 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: Infrared patient thermometer, skin

Meijer by Meijer, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Infrared patient thermometer, skin.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Meijer, Inc.

Sources (1)

  • FDA UDI e9bb5371-01d2-4c18-9b92-80140158e4c7 35 fields · synced May 30, 2026