← Back to catalogue

Solent Proxi

FDA UDI

Class II (US FDA UDI)

by Bayer Healthcare

Identity

Trade Name
SOLENT PROXI FDA UDI
Generic Name
Thrombectomy suction catheter FDA UDI
Device Name
SOLENT PROXI CATH, FG PKG FDA UDI
Model / Reference
109676-001 FDA UDI
Description
SOLENT PROXI CATH, FG PKG FDA UDI

Identifiers

Catalog Number
109676 FDA UDI
Primary DI / UDI-DI
00616258003917 FDA UDI
FDA Product Code
KRA FDA UDI
DXE FDA UDI
GMDN Term
Thrombectomy suction catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1210 FDA UDI
870.5150 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

Yes

FDA UDI

Dimensions & Sizes

Size
Catheter Gauge — 6 French FDA UDI

Category: Thrombectomy suction catheter

Solent Proxi by Bayer Healthcare — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Thrombectomy suction catheter.

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
Bayer Healthcare

Sources (1)

  • FDA UDI f378c96b-f35c-41dc-bb0c-ce9252411d44 36 fields · synced May 31, 2026