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Dr. Talbot's

FDA UDI

Class II (US FDA UDI)

by Talbot's Pharmaceuticals Family Products Llc

Identity

Trade Name
Dr. Talbot's FDA UDI
Generic Name
General-purpose patient temperature probe, reusable FDA UDI
Model / Reference
14900 FDA UDI

Identifiers

Primary DI / UDI-DI
00370797149009 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
General-purpose patient temperature probe, reusable 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: General-purpose patient temperature probe, reusable

Dr. Talbot's by Talbot's Pharmaceuticals Family Products Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose patient temperature probe, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Talbot's Pharmaceuticals Family Products Llc

Sources (1)

  • FDA UDI de7bc99e-7432-4b49-ad75-368cdd56ddef 32 fields · synced May 30, 2026