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Medtronic

FDA UDI

Class II (US FDA UDI)

by Stryker Sustainability Solutions

Identity

Trade Name
Medtronic FDA UDI
Generic Name
Electrical-only medical device connection cable, reprocessed FDA UDI
Device Name
EP CATHETER CABLE 10-PIN FDA UDI
Model / Reference
2ACHC FDA UDI
Description
EP CATHETER CABLE 10-PIN FDA UDI

Identifiers

Catalog Number
2ACHC FDA UDI
Primary DI / UDI-DI
07613327469233 FDA UDI
FDA Product Code
DSA FDA UDI
GMDN Term
Electrical-only medical device connection cable, reprocessed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2900 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Length — 196.0 Centimeter FDA UDI

Category: Electrical-only medical device connection cable, reprocessed

Medtronic by Stryker Sustainability Solutions — 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

Sources (1)

  • FDA UDI c13c3480-bac8-4acf-a2f9-acd81ae84fdd 36 fields · synced Jun 1, 2026