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Profile 3D™

FDA UDIEUDAMED

Class II (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
Profile 3D™ FDA UDI
Generic Name
Mitral/tricuspid annuloplasty ring, open-surgery FDA UDI
Device Name
RING 680R24 PROFILE 3D MEXICO MDR FDA UDI
Model / Reference
680R24 FDA UDI
Description
RING 680R24 PROFILE 3D MEXICO MDR FDA UDI

Identifiers

Primary DI / UDI-DI
00763000661588 FDA UDI
510(k) Number
K073324 FDA UDI
FDA Product Code
KRH FDA UDI
GMDN Term
Mitral/tricuspid annuloplasty ring, open-surgery 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Mitral/tricuspid annuloplasty ring, open-surgery

Profile 3D™ by Medtronic, Inc. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (2)

  • FDA UDI 8318b86d-a1a7-494f-8906-8ac5f2bace0d 37 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 2, 2026