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DiRex™ Steerable Sheath

FDA UDI

Class II (US FDA UDI)

by Oscor Inc.

Identity

Trade Name
DiRex™ Steerable Sheath FDA UDI
Generic Name
Vascular guide-catheter, single-use FDA UDI
Device Name
Steerable sheath, 10F FDA UDI
Model / Reference
M004DS400 FDA UDI
Description
Steerable sheath, 10F FDA UDI

Identifiers

Catalog Number
M004DS400 FDA UDI
Primary DI / UDI-DI
08714729858966 FDA UDI
510(k) Number
K120459 FDA UDI
FDA Product Code
DYB FDA UDI
GMDN Term
Vascular guide-catheter, single-use 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 — 3.6 Millimeter FDA UDI

Category: Vascular guide-catheter, single-use

DiRex™ Steerable Sheath by Oscor Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular guide-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 2a900e0e-0309-41c7-ab3e-9a9cb7a59dbe 38 fields · synced Jun 1, 2026