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SiteSeer™

FDA UDI

Class II (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
SiteSeer™ FDA UDI
Generic Name
Angiographic catheter, single-use FDA UDI
Device Name
CATHETER 4A0019 SS 5PK 4F AL II 100 CM FDA UDI
Model / Reference
4A0019 FDA UDI
Description
CATHETER 4A0019 SS 5PK 4F AL II 100 CM FDA UDI

Identifiers

Primary DI / UDI-DI
00613994894540 FDA UDI
FDA Product Code
DQO FDA UDI
GMDN Term
Angiographic catheter, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1200 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Catheter Gauge — 4.0 French FDA UDI
Lumen/Inner Diameter — 1.07 Millimeter FDA UDI
Length — 100.0 Centimeter FDA UDI

Category: Angiographic catheter, single-use

SiteSeer™ by Medtronic, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Angiographic catheter, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI 0834de9d-b929-4a4a-99cd-b205225f57b2 36 fields · synced May 31, 2026