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QuickClear Thrombectomy System

FDA UDI

Class II (US FDA UDI)

by Volcano AtheroMed Inc.

Identity

Trade Name
QuickClear Thrombectomy System FDA UDI
Generic Name
Thrombectomy suction catheter FDA UDI
Device Name
QuickClear Mechanical Thrombectomy System, 8F, 85 cm, shaped tip FDA UDI
Model / Reference
AC8SH085 FDA UDI
Description
QuickClear Mechanical Thrombectomy System, 8F, 85 cm, shaped tip FDA UDI

Identifiers

Catalog Number
AC8SH085 FDA UDI
Primary DI / UDI-DI
00845225003128 FDA UDI
FDA Product Code
QEZ FDA UDI
GMDN Term
Thrombectomy suction catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5150 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 85 Centimeter FDA UDI

QuickClear Thrombectomy System by Volcano AtheroMed Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1dddcf83-30ce-40cf-b34b-79c8393fed6a 38 fields · synced May 30, 2026