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Adelante S

FDA UDI

Class II (US FDA UDI)

by Oscor Inc.

Identity

Trade Name
Adelante S FDA UDI
Generic Name
Vascular catheter introduction set, nonimplantable FDA UDI
Device Name
Peel-Away Introducer with Hemostatic Valve and Side Port, 9F FDA UDI
Model / Reference
ASU0913B5 FDA UDI
Description
Peel-Away Introducer with Hemostatic Valve and Side Port, 9F FDA UDI

Identifiers

Catalog Number
ASU0913B5 FDA UDI
Primary DI / UDI-DI
10885672104549 FDA UDI
510(k) Number
K073100 FDA UDI
FDA Product Code
DYB FDA UDI
GMDN Term
Vascular catheter introduction set, nonimplantable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1340 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
Lumen/Inner Diameter — 3 Millimeter FDA UDI
Needle Gauge — 18 Gauge FDA UDI

Category: Vascular catheter introduction set, nonimplantable

Adelante S by Oscor Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular catheter introduction set, nonimplantable.

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 4651717a-2358-489a-b194-7bfed8b49792 38 fields · synced Jun 1, 2026