Dlp®

FDA UDI

Class II (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name: DLP® FDA UDI
Generic Name: Coronary sinus cannula FDA UDI
Device Name: CANNULA 30320 COR SIL BODY 20FR 10PK 17L FDA UDI
Model / Reference: 30320 FDA UDI
Description: CANNULA 30320 COR SIL BODY 20FR 10PK 17L FDA UDI

Identifiers

Primary DI / UDI-DI: 20643169454600 FDA UDI
510(k) Number: K141951 FDA UDI
K230960 FDA UDI
K231206 FDA UDI
FDA Product Code: DWF FDA UDI
GMDN Term: Coronary sinus cannula 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Catheter Gauge — 20.0 French FDA UDI

Category: Coronary sinus cannula

Dlp® by Medtronic, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Coronary sinus cannula.

Coronary artery cannula — LivaNova USA, Inc. · Class II
PEAK MEDICAL — PEAK MEDICAL Distribution Inc · Class I
PEAK MEDICAL — PEAK MEDICAL Distribution Inc · Class I
Coronary artery cannula — LivaNova USA, Inc. · Class II
Edwards Lifesciences Retrograde Cardioplegia Catheter — Edwards Lifesciences LLC · Class II
Coronary sinus cannula — LivaNova USA, Inc. · Class II
PEAK MEDICAL — PEAK MEDICAL Distribution Inc · Class I
Coronary artery cannula — LivaNova USA, Inc. · Class II

Cleared under the same submission

K141951 also covers:

DLP® — MEDTRONIC, INC.
DLP® — MEDTRONIC, INC.

K230960 also covers:

DLP® — MEDTRONIC, INC.
DLP® — MEDTRONIC, INC.

K231206 also covers:

DLP® — MEDTRONIC, INC.
DLP® — MEDTRONIC, INC.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Medtronic, Inc.

Sources (1)

FDA UDI de82a97a-0e62-4d07-ae16-9a9dabe19d2a 36 fields · synced May 31, 2026