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Memo 3d

FDA UDI

Class II (US FDA UDI)

by Corcym Inc.

Identity

Trade Name
MEMO 3D FDA UDI
Generic Name
Mitral/tricuspid annuloplasty ring, open-surgery FDA UDI
Model / Reference
SMD36 FDA UDI

Identifiers

Catalog Number
SMD36 FDA UDI
Primary DI / UDI-DI
08022057013156 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Mitral/tricuspid annuloplasty ring, open-surgery

Memo 3d by Corcym 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
Corcym Inc.

Sources (1)

  • FDA UDI 42f181e7-7e7c-4e9f-bf94-78af2a231064 33 fields · synced Jun 6, 2026