Freezpen CL-FP-00

GUDID B386CLFP000

H & O Equipments SA

General cryosurgical system, cryogen gas, mechanical
Primary Device IDB386CLFP000
NIH Device Record Key4c452065-0e17-4b74-ab05-ca2ea11a52b8
Commercial Distribution StatusIn Commercial Distribution
Brand NameFreezpen
Version Model NumberFreezpen
Catalog NumberCL-FP-00
Company DUNS370212933
Company NameH & O Equipments SA
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone888-2482838
Emailinfo@clinic6.com
Phone888-2482838
Emailinfo@clinic6.com
Phone888-2482838
Emailinfo@clinic6.com
Phone888-2482838
Emailinfo@clinic6.com
Phone888-2482838
Emailinfo@clinic6.com
Phone888-2482838
Emailinfo@clinic6.com
Phone888-2482838
Emailinfo@clinic6.com
Phone888-2482838
Emailinfo@clinic6.com
Phone888-2482838
Emailinfo@clinic6.com
Phone888-2482838
Emailinfo@clinic6.com
Phone888-2482838
Emailinfo@clinic6.com
Phone888-2482838
Emailinfo@clinic6.com
Phone888-2482838
Emailinfo@clinic6.com
Phone888-2482838
Emailinfo@clinic6.com
Phone888-2482838
Emailinfo@clinic6.com
Phone888-2482838
Emailinfo@clinic6.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB386CLFP000 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEHUnit, Cryosurgical, Accessories

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-24

On-Brand Devices [Freezpen]

B386CLN2O8GCARTON28g N2O cartridges for Freezpen
B386CLFP000Freezpen

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.