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Chameleon

FDA UDI

Class II (US FDA UDI)

by Av Medical Technologies, Ltd.

Identity

Trade Name
Chameleon FDA UDI
Generic Name
Peripheral angioplasty balloon catheter, basic FDA UDI
Device Name
Chameleon PTA Balloon Dilatation Catheter 12x40 mm FDA UDI
Model / Reference
12x40 FDA UDI
Description
Chameleon PTA Balloon Dilatation Catheter 12x40 mm FDA UDI

Identifiers

Catalog Number
CH12-40-75US FDA UDI
Primary DI / UDI-DI
07290016745085 FDA UDI
FDA Product Code
KRA FDA UDI
LIT FDA UDI
GMDN Term
Peripheral angioplasty balloon catheter, basic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1210 FDA UDI
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

Chameleon by Av Medical Technologies, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral angioplasty balloon catheter, basic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 043ff1c8-f58a-4645-be02-7ae302a4d504 36 fields · synced May 30, 2026