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CorVocet™

FDA UDI

Class II (US FDA UDI)

by Merit Medical Systems, Inc.

Identity

Trade Name
CorVocet™ FDA UDI
Generic Name
Soft-tissue biopsy procedure kit, non-medicated FDA UDI
Model / Reference
00884450316665 FDA UDI

Identifiers

Catalog Number
CORCA2010B/A FDA UDI
Primary DI / UDI-DI
00884450316665 FDA UDI
FDA Product Code
KNW FDA UDI
GMDN Term
Soft-tissue biopsy procedure kit, non-medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1075 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

No

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: Soft-tissue biopsy procedure kit, non-medicated

The CorVocet device is a comprehensive soft tissue biopsy procedure kit designed for medical professionals, particularly gastroenterologists and urologists. It includes a single-use biopsy needle for non-specific procedures, which are typically performed to collect tissue samples for diagnostic purposes.

Similar devices

Also classified as Soft-tissue biopsy procedure kit, non-medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Merit Medical Systems, Inc.

Sources (1)

  • FDA UDI 324539fa-0b27-47be-a379-e7227a6c6c61 34 fields · synced Oct 6, 2026