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Tarry Probes

FDA UDI

Class II (US FDA UDI)

by Tarry Medical Products, Inc.

Identity

Trade Name
Tarry Probes FDA UDI
Generic Name
General-purpose patient temperature probe, single-use FDA UDI
Device Name
T 08730 Single Use Skin Temperature Probe FDA UDI
Model / Reference
T 08730 FDA UDI
Description
T 08730 Single Use Skin Temperature Probe FDA UDI

Identifiers

Catalog Number
T 08730 FDA UDI
Primary DI / UDI-DI
00854758006025 FDA UDI
510(k) Number
K071977 FDA UDI
FDA Product Code
FMT FDA UDI
FMZ FDA UDI
GMDN Term
General-purpose patient temperature probe, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5130 FDA UDI
880.5400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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, single-use

Tarry Probes by Tarry Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose patient temperature probe, single-use.

Cleared under the same submission

K071977 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tarry Medical Products, Inc.

Sources (1)

  • FDA UDI a95f83d9-e66a-4e2b-a2c0-f3c5026987a7 36 fields · synced Jun 9, 2026