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PSG Cable E

FDA UDI

Class II (US FDA UDI)

by Sentec, Inc.

Identity

Trade Name
PSG Cable E FDA UDI
Generic Name
Pulse Co-oximeter probe, reusable FDA UDI
Device Name
The PSG Adapter Cable is intended to interface the SenTec Digital Monitor to Polygraphs (PG) or Polysomnographs (PSG) FDA UDI
Model / Reference
PSG Cable E FDA UDI
Description
The PSG Adapter Cable is intended to interface the SenTec Digital Monitor to Polygraphs (PG) or Polysomnographs (PSG) FDA UDI

Identifiers

Primary DI / UDI-DI
07640121880650 FDA UDI
510(k) Number
K041548 FDA UDI
K071672 FDA UDI
K101690 FDA UDI
K151329 FDA UDI
FDA Product Code
LPP FDA UDI
LKD FDA UDI
KLK FDA UDI
DQA FDA UDI
DPZ FDA UDI
GMDN Term
Pulse Co-oximeter probe, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.2500 FDA UDI
868.2480 FDA UDI
870.2700 FDA UDI
870.2710 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Pulse Co-oximeter probe, reusableTranscutaneous blood gas monitor sensorTranscutaneous blood gas monitoring system

PSG Cable E by Sentec, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Transcutaneous blood gas monitoring system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sentec, Inc.

Sources (1)

  • FDA UDI eff99d6f-28d2-4398-9f56-388c39c04338 34 fields · synced May 30, 2026