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Fischer Cone Biopsy Excisor

FDA UDI

Class II (US FDA UDI)

by CooperSurgical, Inc.

Identity

Trade Name
Fischer Cone Biopsy Excisor FDA UDI
Generic Name
Open-surgery electrosurgical electrode, monopolar, single-use FDA UDI
Device Name
Fischer Cone Biopsy Excisor; Medium FDA UDI
Model / Reference
900-151 FDA UDI
Description
Fischer Cone Biopsy Excisor; Medium FDA UDI

Identifiers

Primary DI / UDI-DI
00888937003710 FDA UDI
510(k) Number
K061651 FDA UDI
FDA Product Code
HGI FDA UDI
GMDN Term
Open-surgery electrosurgical electrode, monopolar, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.4120 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

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

Category: Open-surgery electrosurgical electrode, monopolar, single-use

Fischer Cone Biopsy Excisor by CooperSurgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Open-surgery electrosurgical electrode, monopolar, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 02307e81-dbca-41b9-a8d1-233c1dc50238 34 fields · synced Jun 9, 2026