← Back to catalogue

MYO/WIRE™ Disposable Patient Cable 2.0

FDA UDI

Class II (US FDA UDI)

by A & E Medical Corporation

Identity

Trade Name
MYO/WIRE™ Disposable Patient Cable 2.0 FDA UDI
Generic Name
Electrical-only medical device connection cable, single-use FDA UDI
Device Name
Disposable Patient Cable, 1 per pouch FDA UDI
Model / Reference
019-540 FDA UDI
Description
Disposable Patient Cable, 1 per pouch FDA UDI

Identifiers

Primary DI / UDI-DI
10841291105282 FDA UDI
FDA Product Code
IKD FDA UDI
GMDN Term
Electrical-only medical device connection cable, single-use 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

No

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, single-use

MYO/WIRE™ Disposable Patient Cable 2.0 by A & E Medical Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

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
A & E Medical Corporation

Sources (1)

  • FDA UDI d3f1a0d3-88b0-4edb-811b-cf244e705641 33 fields · synced Jun 6, 2026