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SteadyTemp

FDA UDIEUDAMED

Class II (US FDA UDI)

by SteadySense GmbH

Identity

Trade Name
SteadyTemp FDA UDI
Generic Name
Wireless patient thermometer, single-use FDA UDI
Model / Reference
1 FDA UDI

Identifiers

Primary DI / UDI-DI
09120095900281 FDA UDI
510(k) Number
K233280 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
Wireless patient thermometer, 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

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Wireless patient thermometer, single-use

SteadyTemp by SteadySense GmbH — Class II — MDR, MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Wireless patient thermometer, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

European Union Unknown

MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
SteadySense GmbH

Sources (2)

  • FDA UDI 820f6460-50a0-409c-ad67-767b3ec60c20 34 fields · synced Jun 19, 2026
  • EUDAMED 1 fields · synced Jun 19, 2026