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Tri-Ad™

FDA UDI

Class II (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
Tri-Ad™ FDA UDI
Generic Name
Heart valve annulus sizer, reusable FDA UDI
Device Name
7900PS TRI-AD 2.0 ADAMS SIZER SET FDA UDI
Model / Reference
7900PS FDA UDI
Description
7900PS TRI-AD 2.0 ADAMS SIZER SET FDA UDI

Identifiers

Primary DI / UDI-DI
00763000102296 FDA UDI
FDA Product Code
KRH FDA UDI
GMDN Term
Heart valve annulus sizer, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.3800 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Heart valve annulus sizer, reusable

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

Similar devices

Also classified as Heart valve annulus sizer, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI 40e79e37-f555-4e31-bf38-e7d7cd7ff455 35 fields · synced May 31, 2026