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Mulit-Snare

FDA UDI

Class II (US FDA UDI)

by PFM medical mepro GmbH

Identity

Trade Name
Mulit-Snare FDA UDI
Generic Name
Intravascular extraction catheter-snare FDA UDI
Device Name
Multi-Snare Micro Set 2mm x 175cm FDA UDI
Model / Reference
147302 FDA UDI
Description
Multi-Snare Micro Set 2mm x 175cm FDA UDI

Identifiers

Primary DI / UDI-DI
04042301061805 FDA UDI
510(k) Number
K011783 FDA UDI
FDA Product Code
DXE FDA UDI
GMDN Term
Intravascular extraction catheter-snare FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5150 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Intravascular extraction catheter-snare

Mulit-Snare by PFM medical mepro GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intravascular extraction catheter-snare.

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 ca1cd413-1a41-4735-ab90-ba60e298b9c5 35 fields · synced May 30, 2026