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OptiMap™ System Interconnect Cable

FDA UDI

Class II (US FDA UDI)

by Cortex, Inc.

Identity

Trade Name
OptiMap™ System Interconnect Cable FDA UDI
Generic Name
Electrical-only medical device connection cable, reprocessed FDA UDI
Device Name
OptiMap™ System Interconnect Cable FDA UDI
Model / Reference
FG0005 FDA UDI
Description
OptiMap™ System Interconnect Cable FDA UDI

Identifiers

Catalog Number
OPTI-SIC FDA UDI
Primary DI / UDI-DI
00850064686098 FDA UDI
FDA Product Code
IKD FDA UDI
GMDN Term
Electrical-only medical device connection cable, reprocessed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.1175 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrical-only medical device connection cable, reprocessed

OptiMap™ System Interconnect Cable by Cortex, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrical-only medical device connection cable, reprocessed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cortex, Inc.

Sources (1)

  • FDA UDI c0d91ce1-049e-4c12-b058-97a93260a110 34 fields · synced Jun 8, 2026