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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Infrared patient thermometer, ear FDA UDI
Device Name
THERMOMETER,EAR,W/EASY PROBE RELEASE FDA UDI
Model / Reference
MDS9700 FDA UDI
Description
THERMOMETER,EAR,W/EASY PROBE RELEASE FDA UDI

Identifiers

Catalog Number
MDS9700 FDA UDI
Primary DI / UDI-DI
00080196310268 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
Infrared patient thermometer, ear 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

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Infrared patient thermometer, ear

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

Similar devices

Also classified as Infrared patient thermometer, ear.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6d10cb02-dad4-47b2-9804-363963521cda 35 fields · synced Jun 8, 2026