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Dlp®

FDA UDI

Class II (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
DLP® FDA UDI
Generic Name
Cardioplegia solution administration adaptor FDA UDI
Device Name
ADAPTER 10003 Y TYPE 20PK 17L FDA UDI
Model / Reference
10003 FDA UDI
Description
ADAPTER 10003 Y TYPE 20PK 17L FDA UDI

Identifiers

Primary DI / UDI-DI
20613994808022 FDA UDI
FDA Product Code
DTL FDA UDI
GMDN Term
Cardioplegia solution administration adaptor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4290 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cardioplegia solution administration adaptor

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

Similar devices

Also classified as Cardioplegia solution administration adaptor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI 31ea5dd0-db5e-42ec-87fe-766ac728778a 34 fields · synced Jun 8, 2026