← Back to catalogue

Cordis ExoSeal Vascular Closure Device

FDA UDI

Class III (US FDA UDI)

by Cordis US Corp.

Identity

Trade Name
Cordis ExoSeal Vascular Closure Device FDA UDI
Generic Name
Femoral artery closure plug/patch, synthetic polymer FDA UDI
Model / Reference
EX500 FDA UDI

Identifiers

Catalog Number
EX500 FDA UDI
Primary DI / UDI-DI
10705032058872 FDA UDI
FDA Product Code
MGB FDA UDI
GMDN Term
Femoral artery closure plug/patch, synthetic polymer FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Femoral artery closure plug/patch, synthetic polymer

Cordis ExoSeal Vascular Closure Device by Cordis US Corp. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Femoral artery closure plug/patch, synthetic polymer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Cordis US Corp.

Sources (1)

  • FDA UDI 4eb4f0d7-524d-4929-8c84-93d567fdc279 34 fields · synced Jun 6, 2026