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Crow's Nest Biopsy Catchment System

FDA UDI

Class I (US FDA UDI)

by Corramedical Inc.

Identity

Trade Name
Crow's Nest Biopsy Catchment System FDA UDI
Generic Name
Blood/tissue storage/culture container FDA UDI
Device Name
Device for segregating and collecting dislodged tumor cells created during a core needle biopsy, sterile FDA UDI
Model / Reference
1 FDA UDI
Description
Device for segregating and collecting dislodged tumor cells created during a core needle biopsy, sterile FDA UDI

Identifiers

Catalog Number
CNBOX1CST FDA UDI
Primary DI / UDI-DI
G669CNBOX1CST0 FDA UDI
FDA Product Code
KDT FDA UDI
GMDN Term
Blood/tissue storage/culture container FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3250 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

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

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
Height — 12.4 Centimeter FDA UDI

Category: Blood/tissue storage/culture container

Crow's Nest Biopsy Catchment System by Corramedical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood/tissue storage/culture container.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Corramedical Inc.

Sources (1)

  • FDA UDI e99840e1-ef18-44d7-955d-0aa4063edecb 37 fields · synced May 31, 2026