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Fiber Optic Temperature Sensor Core

FDA UDI

Class II (US FDA UDI)

by MIPM Mammendorfer Institut für Physik und Medizin GmbH

Identity

Trade Name
Fiber Optic Temperature Sensor Core FDA UDI
Generic Name
General-purpose patient temperature probe, reusable FDA UDI
Model / Reference
Fiber Optic Temperature Sensor Core FDA UDI

Identifiers

Catalog Number
6210031 FDA UDI
Primary DI / UDI-DI
04255629200720 FDA UDI
510(k) Number
K142032 FDA UDI
FDA Product Code
MWI FDA UDI
GMDN Term
General-purpose patient temperature probe, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2300 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: General-purpose patient temperature probe, reusable

Fiber Optic Temperature Sensor Core by MIPM Mammendorfer Institut für Physik und Medizin GmbH — Class II — FDA UDI — listed in FDA GUDID

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 49700590-8019-4976-9f12-a2fe1c9c3b26 35 fields · synced May 30, 2026