Single Use Biopsy Forceps FB-433D

GUDID 14953170394536

OLYMPUS MEDICAL SYSTEMS CORP.

Flexible endoscopic biopsy forceps, single-use Flexible endoscopic biopsy forceps, single-use Flexible endoscopic biopsy forceps, single-use Flexible endoscopic biopsy forceps, single-use Flexible endoscopic biopsy forceps, single-use Flexible endoscopic biopsy forceps, single-use Flexible endoscopic biopsy forceps, single-use Flexible endoscopic biopsy forceps, single-use Flexible endoscopic biopsy forceps, single-use Flexible endoscopic biopsy forceps, single-use Flexible endoscopic biopsy forceps, single-use Flexible endoscopic biopsy forceps, single-use Flexible endoscopic biopsy forceps, single-use Flexible endoscopic biopsy forceps, single-use Flexible endoscopic biopsy forceps, single-use Flexible endoscopic biopsy forceps, single-use Flexible endoscopic biopsy forceps, single-use Flexible endoscopic biopsy forceps, single-use Flexible endoscopic biopsy forceps, single-use Flexible endoscopic biopsy forceps, single-use Flexible endoscopic biopsy forceps, single-use Flexible endoscopic biopsy forceps, single-use Flexible endoscopic biopsy forceps, single-use Flexible endoscopic biopsy forceps, single-use Flexible endoscopic biopsy forceps, single-use Flexible endoscopic biopsy forceps, single-use Flexible endoscopic biopsy forceps, single-use Flexible endoscopic biopsy forceps, single-use
Primary Device ID14953170394536
NIH Device Record Key190c93ff-c080-42db-a7a1-25baf53f80d9
Commercial Distribution StatusIn Commercial Distribution
Brand NameSingle Use Biopsy Forceps FB-433D
Version Model NumberFB-433D
Company DUNS711789789
Company NameOLYMPUS MEDICAL SYSTEMS CORP.
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS104953170394539 [Primary]
GS114953170394536 [Package]
Contains: 04953170394539
Package: [4 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

EOQBronchoscope (Flexible Or Rigid)

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-12-27
Device Publish Date2021-12-17

On-Brand Devices [Single Use Biopsy Forceps FB-433D]

14953170401951FB-433D
14953170394536FB-433D

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