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Dlp®

FDA UDI

Class II (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
DLP® FDA UDI
Generic Name
Coronary artery perfusion catheter FDA UDI
Device Name
CANNULA 30023 VESS RAD BLUNT 3MM 40P 17L FDA UDI
Model / Reference
30023 FDA UDI
Description
CANNULA 30023 VESS RAD BLUNT 3MM 40P 17L FDA UDI

Identifiers

Primary DI / UDI-DI
20613994646068 FDA UDI
510(k) Number
K810820 FDA UDI
FDA Product Code
DWF FDA UDI
GMDN Term
Coronary artery perfusion catheter 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

No

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

No

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
Outer Diameter — 3.0 Millimeter FDA UDI

Category: Coronary artery perfusion catheter

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

Similar devices

Also classified as Coronary artery perfusion catheter.

Cleared under the same submission

K810820 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI 797e988f-24a2-430c-87d6-848c57c1a672 36 fields · synced Jun 8, 2026