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Multi-Snare®

FDA UDI

Class II (US FDA UDI)

by B Braun Interventional Systems, Inc

Identity

Trade Name
Multi-Snare® FDA UDI
Generic Name
Intravascular extraction catheter-snare FDA UDI
Device Name
MULTI-SNARE 30MMX125CM W/6FRX105CM FDA UDI
Model / Reference
612976 FDA UDI
Description
MULTI-SNARE 30MMX125CM W/6FRX105CM FDA UDI

Identifiers

Catalog Number
612976 FDA UDI
Primary DI / UDI-DI
04046964349416 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
Not 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Multi-Snare® by B Braun Interventional Systems, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K011783 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
B Braun Interventional Systems, Inc

Sources (1)

  • FDA UDI ecdfa6eb-4756-4cc6-a90d-28cc785be981 38 fields · synced May 31, 2026