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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE FDA UDI
Generic Name
Electrical-only medical device connection cable, reprocessed FDA UDI
Device Name
OCTARAY CARTO INTERFACE CABLE, 10FT FDA UDI
Model / Reference
D134402RH FDA UDI
Description
OCTARAY CARTO INTERFACE CABLE, 10FT FDA UDI

Identifiers

Catalog Number
D134402RH FDA UDI
Primary DI / UDI-DI
10197344161768 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrical-only medical device connection cable, reprocessed

Medline by Medline Industries, 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
Medline Industries, Inc.

Sources (1)

  • FDA UDI 9d781510-99c7-40c5-b72b-d09260f5412b 35 fields · synced May 31, 2026