SPHERZ: ILUMARK NONSTERILE 1010-05

GUDID 00815212025624

Izi Medical Products, LLC

Radiographic image marker, manual
Primary Device ID00815212025624
NIH Device Record Key52acfc4f-eca7-480b-996c-4103d2995ded
Commercial Distribution StatusIn Commercial Distribution
Brand NameSPHERZ: ILUMARK NONSTERILE 1010-05
Version Model Number1010-05
Company DUNS933506164
Company NameIzi Medical Products, LLC
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100815212025624 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HAWNeurological Stereotaxic Instrument

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-05-26
Device Publish Date2022-05-18

Devices Manufactured by Izi Medical Products, LLC

00815212026935 - Duro-Ject Bone Cement Injection Tube2024-10-22
00815212026911 - KIT:BALLOON AND BONE FILLER2024-09-05
00815212026928 - KIT:BALLOON,FILLER,ACCESS,DRILL2024-09-05
10815212026895 - OsteoPearl Vertebral Balloon (15mm), 10G2024-08-13
00815212026904 - OsteoPearl Vertebral Balloon (15mm) & Inflation Device Kit, 10G2024-08-13
00815212024467 - STRYKER NAVIGATED BIOPSY NEEDLE2024-08-07
00815212026874 - BKP-10-12.0-15.0-A2024-07-08
00815212026881 - BKP-11-12.0-15.0-A2024-07-08

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