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Angios Classic Angiographic Catheter

FDA UDI

Class II (US FDA UDI)

by Oscor Inc.

Identity

Trade Name
Angios Classic Angiographic Catheter FDA UDI
Generic Name
Angiographic catheter, single-use FDA UDI
Device Name
Angiographic Catheter, PIGTAIL 145°, 5F, 17 mm FDA UDI
Model / Reference
ANG1-0797 FDA UDI
Description
Angiographic Catheter, PIGTAIL 145°, 5F, 17 mm FDA UDI

Identifiers

Catalog Number
ANG1-0797 FDA UDI
Primary DI / UDI-DI
50836559008748 FDA UDI
510(k) Number
K092118 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 80 Centimeter FDA UDI

Category: Angiographic catheter, single-use

Angios Classic Angiographic Catheter by Oscor Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Angiographic catheter, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Oscor Inc.

Sources (1)

  • FDA UDI 44b06c96-9844-43e1-bd02-ed147692c409 38 fields · synced May 30, 2026