← Back to catalogue

TYSHAK Mini®

FDA UDI

Class II (US FDA UDI)

by B Braun Interventional Systems, Inc

Identity

Trade Name
TYSHAK Mini® FDA UDI
Generic Name
Cardiac valvuloplasty catheter FDA UDI
Device Name
PDC406 TYSHAK MINI 10MM 2CM FDA UDI
Model / Reference
611991 FDA UDI
Description
PDC406 TYSHAK MINI 10MM 2CM FDA UDI

Identifiers

Catalog Number
611991 FDA UDI
Primary DI / UDI-DI
04046964339752 FDA UDI
510(k) Number
K003276 FDA UDI
FDA Product Code
DQY FDA UDI
LIT FDA UDI
GMDN Term
Cardiac valvuloplasty catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1250 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

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

Category: Cardiac valvuloplasty catheter

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

Similar devices

Also classified as Cardiac valvuloplasty catheter.

Cleared under the same submission

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

Sources (1)

  • FDA UDI 0c3f0bd5-ce0d-48df-a3e1-e4a1842e38df 37 fields · synced May 31, 2026