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Aviator

FDA UDI

Class II (US FDA UDI)

by Cordis US Corp.

Identity

Trade Name
AVIATOR FDA UDI
Generic Name
Peripheral angioplasty balloon catheter, basic FDA UDI
Device Name
AVIATOR PLUS .014 6.0X15 142CM FDA UDI
Model / Reference
4246015W FDA UDI
Description
AVIATOR PLUS .014 6.0X15 142CM FDA UDI

Identifiers

Catalog Number
4246015W FDA UDI
Primary DI / UDI-DI
20705032005897 FDA UDI
510(k) Number
K071189 FDA UDI
FDA Product Code
LIT FDA UDI
GMDN Term
Peripheral angioplasty balloon catheter, basic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1250 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Peripheral angioplasty balloon catheter, basic

Aviator by Cordis US Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral angioplasty balloon catheter, basic.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cordis US Corp.

Sources (1)

  • FDA UDI 22078b22-8f33-4abe-9c09-42271ab2f887 36 fields · synced Jun 8, 2026