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Bio-Medicus™

FDA UDI

Class II (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
Bio-Medicus™ FDA UDI
Generic Name
Mitral/tricuspid annuloplasty ring, open-surgery FDA UDI
Device Name
CANNULA CB96835-008 BIO-MEDICUS 8FR FDA UDI
Model / Reference
CB96835-008 FDA UDI
Description
CANNULA CB96835-008 BIO-MEDICUS 8FR FDA UDI

Identifiers

Primary DI / UDI-DI
00763000193577 FDA UDI
FDA Product Code
DWF FDA UDI
GMDN Term
Mitral/tricuspid annuloplasty ring, open-surgery FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4210 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

Yes

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

No

FDA UDI

Dimensions & Sizes

Size
Length — 10.0 Centimeter FDA UDI
Catheter Gauge — 8.0 French FDA UDI

Category: Mitral/tricuspid annuloplasty ring, open-surgery

Bio-Medicus™ by Medtronic, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mitral/tricuspid annuloplasty ring, open-surgery.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI be7249fa-26a5-4d7a-85e0-4630eb0149ca 36 fields · synced Jun 1, 2026