← Back to catalogue

Medistim Interconnect Cable

FDA UDI

Class II (US FDA UDI)

by Medi-Stim Asa

Identity

Trade Name
Medistim Interconnect Cable FDA UDI
Generic Name
Invasive vascular ultrasound system FDA UDI
Model / Reference
CV200111 FDA UDI

Identifiers

Catalog Number
CV200111 FDA UDI
Primary DI / UDI-DI
07070554104298 FDA UDI
510(k) Number
K040228 FDA UDI
FDA Product Code
IYN FDA UDI
DPW FDA UDI
GMDN Term
Invasive vascular ultrasound system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1550 FDA UDI
870.2100 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

Category: Invasive vascular ultrasound system

Medistim Interconnect Cable by Medi-Stim Asa — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Invasive vascular ultrasound system.

Cleared under the same submission

K040228 also covers:

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
Medi-Stim Asa

Sources (1)

  • FDA UDI dafc0ef4-4381-4ccb-b8c2-4ceb878aed96 34 fields · synced Jun 1, 2026