← Back to catalogue

Fore-Sight Elite®

FDA UDI

Class II (US FDA UDI)

by Cas Medical Systems, Inc.

Identity

Trade Name
FORE-SIGHT ELITE® FDA UDI
Generic Name
Tissue saturation oximeter sensor, single-use FDA UDI
Device Name
Tissue Oximeter Sensor (Non adhesive Small) FDA UDI
Model / Reference
01-07-1100 FDA UDI
Description
Tissue Oximeter Sensor (Non adhesive Small) FDA UDI

Identifiers

Primary DI / UDI-DI
10609538711005 FDA UDI
510(k) Number
K143675 FDA UDI
FDA Product Code
MUD FDA UDI
GMDN Term
Tissue saturation oximeter sensor, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2700 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Height — 2.5 Centimeter FDA UDI

Category: Tissue saturation oximeter sensor, single-use

Fore-Sight Elite® by Cas Medical Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tissue saturation oximeter sensor, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 47edf014-d418-450c-9fab-a717558e4c74 35 fields · synced May 30, 2026