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SourceMark

FDA UDI

Class II (US FDA UDI)

by Sourcemark, Llc.

Identity

Trade Name
SourceMark FDA UDI
Generic Name
General-purpose patient temperature probe, single-use FDA UDI
Model / Reference
SMC400-MP-M FDA UDI

Identifiers

Primary DI / UDI-DI
00813799006760 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
General-purpose patient temperature probe, single-use 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General-purpose patient temperature probe, single-use

SourceMark by Sourcemark, Llc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sourcemark, Llc.

Sources (1)

  • FDA UDI 36bf7374-6ed0-4ee1-90c3-570e7e63af40 32 fields · synced May 30, 2026