← Back to catalogue

Perceval S Single Use Accessory Kit

FDA UDI

by Corcym Srl

Identity

Trade Name
Perceval S Single Use Accessory Kit FDA UDI
Generic Name
Self-expandable heart valve prosthesis post-dilation balloon catheter FDA UDI
Model / Reference
ICV1346 FDA UDI

Identifiers

Primary DI / UDI-DI
08022057015228 FDA UDI
GMDN Term
Self-expandable heart valve prosthesis post-dilation balloon catheter FDA UDI

Classification

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

Yes

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

Category: Heart valve prosthesis holder, single-useSelf-expandable heart valve bioprosthesis collapsing tool, single-useSelf-expandable heart valve prosthesis post-dilation balloon catheter

Perceval S Single Use Accessory Kit by Corcym Srl — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Self-expandable heart valve bioprosthesis collapsing tool, single-use.

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
Corcym Srl

Sources (1)

  • FDA UDI 5749c60c-0b68-4cab-975b-c8ed422711c9 32 fields · synced Jun 1, 2026