← Back to catalogue

Launcher

FDA UDI

Class II (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
Launcher FDA UDI
Generic Name
Vascular guide-catheter, single-use FDA UDI
Device Name
CATHETER LA6JL40A LA 6F 110CM JL40 FDA UDI
Model / Reference
LA6JL40A FDA UDI
Description
CATHETER LA6JL40A LA 6F 110CM JL40 FDA UDI

Identifiers

Primary DI / UDI-DI
00613994179388 FDA UDI
510(k) Number
K021256 FDA UDI
FDA Product Code
DQY FDA UDI
GMDN Term
Vascular guide-catheter, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1250 FDA UDI
Commercial Distribution
Not 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 110.0 Centimeter FDA UDI
Catheter Gauge — 6.0 French FDA UDI

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

Cleared under the same submission

K021256 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI 349f3ad8-083c-4f4f-87c7-744a73ffdc34 38 fields · synced May 31, 2026