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Starboard Temperature Probes

FDA UDI

Class II (US FDA UDI)

by Starboard Medical, Inc.

Identity

Trade Name
Starboard Temperature Probes FDA UDI
Generic Name
Electronic oesophageal stethoscope, single-use FDA UDI
Device Name
Esophageal Stethoscope with 400 Series Temperature Sensor, 24 Fr. FDA UDI
Model / Reference
40024-ES FDA UDI
Description
Esophageal Stethoscope with 400 Series Temperature Sensor, 24 Fr. FDA UDI

Identifiers

Catalog Number
40024-ES FDA UDI
Primary DI / UDI-DI
00850933007054 FDA UDI
510(k) Number
K111050 FDA UDI
FDA Product Code
BZT FDA UDI
GMDN Term
Electronic oesophageal stethoscope, 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electronic oesophageal stethoscope, single-use

Starboard Temperature Probes by Starboard Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electronic oesophageal stethoscope, single-use.

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 1a528182-ba13-457d-9e3d-35d948f825b5 35 fields · synced May 30, 2026