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LAM Fixation Standard

FDA UDI

Class II (US FDA UDI)

by Compumedics Germany GmbH

Identity

Trade Name
LAM Fixation Standard FDA UDI
Generic Name
Noninvasive vascular ultrasound system probe FDA UDI
Device Name
LAM Sets Standard unilateral with 1 MHz probe, click&stay FDA UDI
Model / Reference
FIx_LAM_S_7498 FDA UDI
Description
LAM Sets Standard unilateral with 1 MHz probe, click&stay FDA UDI

Identifiers

Catalog Number
7498 FDA UDI
Primary DI / UDI-DI
04260493311748 FDA UDI
510(k) Number
K051085 FDA UDI
FDA Product Code
ITX FDA UDI
GMDN Term
Noninvasive vascular ultrasound system probe FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1570 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Noninvasive vascular ultrasound system probe

LAM Fixation Standard by Compumedics Germany GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Noninvasive vascular ultrasound system probe.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f224b75a-3f9d-4b79-96f1-3f43b567bf85 36 fields · synced Jun 1, 2026