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Aspirex® S 10F 110cm

FDA UDI

Class II (US FDA UDI)

by Straub Medical AG

Identity

Trade Name
Aspirex® S 10F 110cm FDA UDI
Generic Name
Thrombectomy rotational catheter FDA UDI
Device Name
The Aspirex® S catheter (gauge 10F; length 110cm) is over-the-wire, single use, percutaneous device for the treatment of occlusions in venous vasculature. FDA UDI
Model / Reference
80211 FDA UDI
Description
The Aspirex® S catheter (gauge 10F; length 110cm) is over-the-wire, single use, percutaneous device for the treatment of occlusions in venous vasculature. FDA UDI

Identifiers

Catalog Number
80211 FDA UDI
Primary DI / UDI-DI
07640142810506 FDA UDI
510(k) Number
K220270 FDA UDI
FDA Product Code
QEW FDA UDI
GMDN Term
Thrombectomy rotational 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
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Catheter Gauge — 10 French FDA UDI
Catheter Working Length — 110 Centimeter FDA UDI

Aspirex® S 10F 110cm by Straub Medical AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K220270 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Straub Medical AG

Sources (1)

  • FDA UDI 9188dfba-3b93-42ca-92c8-cb9f86534f66 38 fields · synced May 30, 2026