← Back to catalogue

VisiSheath Dilator Sheath

EUDAMEDFDA UDI

Class III (EU MDR)

Ref 501-112

by Spectranetics Corporation

Identity

Trade Name
VisiSheath Dilator Sheath EUDAMEDFDA UDI
Generic Name
Vascular dilator, single-use FDA UDI
Device Name
VisiSheath Dilator Sheath EUDAMED
Model / Reference
501-112 EUDAMEDFDA UDI

Identifiers

Catalog Number
501-112 FDA UDI
Primary DI / UDI-DI
00813132020385 EUDAMEDFDA UDI
Basic UDI-DI
B-00813132020385 EUDAMED
FDA Product Code
DRE FDA UDI
EMDN Code
C9002 VASCULAR AND FASCIAL DILATORS EUDAMED
GMDN Term
Vascular dilator, single-use FDA UDI

Classification

Device Class
Class III EUDAMED
Class II FDA UDI
Regulation Number
870.1310 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI

Dimensions & Sizes

Size
Lumen/Inner Diameter — 4.2 Millimeter FDA UDI
Length — 33 Centimeter FDA UDI

Category: Fascial tissue dilator, single-use

VisiSheath Dilator Sheath by Spectranetics Corporation — Class III — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fascial tissue dilator, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
US-MF-000020669
Authorised Representative
Spectranetics International B.V. NL-AR-000001484

Sources (2)

  • EUDAMED 1836f072-3dbc-4b38-96ec-d5dc1553b968 61 fields · synced Jul 11, 2026
  • FDA UDI 9474e18e-2d9d-4c2c-ae70-68ea9601a59a 36 fields · synced May 29, 2026