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Source Abroad

FDA UDI

Class II (US FDA UDI)

by Broder Bros., Co.

Identity

Trade Name
Source Abroad FDA UDI
Generic Name
Intermittent electronic patient thermometer FDA UDI
Device Name
PL-2335 Digital Thermometer Source Abroad overseas direct product Plastic digital thermometer in plastic box FDA approved Price includes PMS match color trim COLOR: WRED FDA UDI
Model / Reference
PL-2335 FDA UDI
Description
PL-2335 Digital Thermometer Source Abroad overseas direct product Plastic digital thermometer in plastic box FDA approved Price includes PMS match color trim COLOR: WRED FDA UDI

Identifiers

Catalog Number
PL-2335 FDA UDI
Primary DI / UDI-DI
00030028000089 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

Yes

FDA UDI

Category: Intermittent electronic patient thermometer

Source Abroad by Broder Bros., Co. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intermittent electronic patient thermometer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Broder Bros., Co.

Sources (1)

  • FDA UDI 88dfa99c-ae2d-4026-903f-9b49763b9dd7 35 fields · synced Jun 8, 2026