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St3304

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 07-10-00Model ST3304

by Shenzhen SINO-K Medical Technology Co., Ltd.

Identity

Trade Name
ST3304 EUDAMED
SINO-K FDA UDI
Generic Name
General-purpose patient temperature probe, reusable FDA UDI
Device Name
Temperature Probe EUDAMED
Skin contact Temperature Probe, pediatric, reusable FDA UDI
Model / Reference
ST3304 EUDAMEDFDA UDI
07-10-00 EUDAMED
Description
Skin contact Temperature Probe, pediatric, reusable FDA UDI

Identifiers

Primary DI / UDI-DI
06972820961103 EUDAMEDFDA UDI
Basic UDI-DI
B-06972820961103 EUDAMED
510(k) Number
K223807 FDA UDI
FDA Product Code
FLL FDA UDI
EMDN Code
V03010201 TEMPERATURE MONITORING CUTANEOUS PROBES EUDAMED
GMDN Term
General-purpose patient temperature probe, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
880.2910 FDA UDI
Market of Registration
Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General-purpose patient temperature probe, reusable

St3304 by Shenzhen SINO-K Medical Technology Co., Ltd. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
CN-MF-000021157
Authorised Representative
Prolinx GmbH DE-AR-000005129

Sources (2)

  • EUDAMED 280fba4e-cc4d-4f7e-8af6-1e4de2595d7c 61 fields · synced Jul 14, 2026
  • FDA UDI 93e7b6ba-26fb-43ab-bc78-b0f9cf786f59 34 fields · synced May 30, 2026