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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
00884450373750 FDA UDI

Identifiers

Catalog Number
CORC2020B FDA UDI
Primary DI / UDI-DI
00884450373750 FDA UDI
FDA Product Code
FCG 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

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

Category: Soft-tissue biopsy procedure kit, non-medicated

Unlock the benefits of the CorVocet Biopsy Needle System with Merit Medical Systems, Inc., a leading developer and manufacturer of innovative medical devices. This single-use biopsy needle is designed for patients undergoing soft tissue biopsies, providing precise and accurate results. Developed in collaboration with leading gastroenterology and urology experts, the CorVocet system ensures optimal performance and minimizes complications.

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 b6842b81-ef88-4e87-8470-086b283b25c7 34 fields · synced Oct 6, 2026