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ClosureFast Introducer Sheath

FDA UDI

Class II (US FDA UDI)

by Argon Medical Devices, Inc.

Identity

Trade Name
ClosureFast Introducer Sheath FDA UDI
Generic Name
Vascular catheter introduction set, nonimplantable FDA UDI
Device Name
ClosureFast™ Introducer Sheath Set 7Fr/Ch (2.3mm) x 11cm FDA UDI
Model / Reference
IS-7F11 FDA UDI
Description
ClosureFast™ Introducer Sheath Set 7Fr/Ch (2.3mm) x 11cm FDA UDI

Identifiers

Catalog Number
IS-7F11 FDA UDI
Primary DI / UDI-DI
00886333227525 FDA UDI
510(k) Number
K780126 FDA UDI
FDA Product Code
DRE FDA UDI
GMDN Term
Vascular catheter introduction set, nonimplantable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1310 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

Category: Vascular catheter introduction set, nonimplantable

ClosureFast Introducer Sheath by Argon Medical Devices, 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

Sources (1)

  • FDA UDI efe9f290-b293-4fb2-8aad-33bb9a0ae1b3 38 fields · synced Jun 9, 2026