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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
SM4503NP FDA UDI

Identifiers

Primary DI / UDI-DI
00813799004797 FDA UDI
FDA Product Code
BZT FDA UDI
GMDN Term
General-purpose patient temperature probe, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1920 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 d272db16-c4a8-4180-9324-f7f2e0937e9a 32 fields · synced Jun 1, 2026