Anchor 90 Deg Ball Probe, 1.7 mm Dia

GUDID 00685447002055

Baylis Médicale Cie Inc

Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use Exploratory blunt needle, single-use
Primary Device ID00685447002055
NIH Device Record Keyb6cce3fd-d36c-463c-8dd5-3e7789d871e4
Commercial Distribution StatusIn Commercial Distribution
Brand NameAnchor 90 Deg Ball Probe, 1.7 mm Dia
Version Model NumberPSZ-400-300
Company DUNS249225954
Company NameBaylis Médicale Cie Inc
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100685447002055 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HRXArthroscope

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2017-06-16

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00685447019060 - VersaCross Connect Access Solution for FARADRIVE2024-01-19 1 x VersaCross Connect Transseptal Dilator; 1 x VersaCross RF Wire (including 1 x Connector Cable (Single Use))
00685447019077 - VersaCross Connect Access Solution for FARADRIVE2024-01-19 1 x VersaCross Connect Transseptal Dilator; 1 x VersaCross RF Wire (including 1 x Connector Cable (Single Use))
00685447005964 - SupraCross Steerable Sheath2023-11-16 SupraCross Steerable Sheath; Transseptal Dilator; J-Tip Guidewire
00685447005971 - SupraCross Steerable Sheath2023-11-16 SupraCross Steerable Sheath; Transseptal Dilator; J-Tip Guidewire
00685447005988 - SupraCross Steerable Sheath2023-11-16 SupraCross Steerable Sheath; Transseptal Dilator; J-Tip Guidewire
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