← Back to catalogue

Monitor Input Cable, Mikro-Cath to EP-Tracer System

FDA UDI

Class II (US FDA UDI)

by Millar LLC.

Identity

Trade Name
Monitor Input Cable, Mikro-Cath to EP-Tracer System FDA UDI
Generic Name
Transducer signal amplifier FDA UDI
Device Name
The 850-5148 cable is designed as an interface between the Millar Mikro-CathTM catheter (Part #825-0101-5), and the Schwarzer Cardiotek GmbH medical device as detailed below: EP-Tracer 38, EP-Tracer 70, EP-Tracer 102, when used with the following system configurations: EP-Tracer Portable, EP-Tracer Stationary, EP-Tracer ProCart. The 850-5148 cable is 10 feet long. The cable is supplied nonsterile. FDA UDI
Model / Reference
850-5148 FDA UDI
Description
The 850-5148 cable is designed as an interface between the Millar Mikro-CathTM catheter (Part #825-0101-5), and the Schwarzer Cardiotek GmbH medical device as detailed below: EP-Tracer 38, EP-Tracer 70, EP-Tracer 102, when used with the following system configurations: EP-Tracer Portable, EP-Tracer Stationary, EP-Tracer ProCart. The 850-5148 cable is 10 feet long. The cable is supplied nonsterile. FDA UDI

Identifiers

Catalog Number
850-5148 FDA UDI
Primary DI / UDI-DI
00868924000267 FDA UDI
FDA Product Code
DRQ FDA UDI
GMDN Term
Transducer signal amplifier FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2060 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Transducer signal amplifier

Monitor Input Cable, Mikro-Cath to EP-Tracer System by Millar LLC. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Transducer signal amplifier.

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

Manufacturer
Millar LLC.

Sources (1)

  • FDA UDI e41207bd-51e8-4dbb-a898-322ff143426d 36 fields · synced Jun 8, 2026