Primary Device ID | 00815212020421 |
NIH Device Record Key | 660b5c3a-dfba-4182-8980-e4d6cc478714 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Threaded Spherz |
Version Model Number | TS2002 |
Company DUNS | 933506164 |
Company Name | Izi Medical Products, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00815212020421 [Primary] |
HAW | Neurological Stereotaxic Instrument |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-11-10 |
00815212021565 | 2020-40 |
00815212021558 | 2020-160 |
00815212021541 | 2020-130 |
00815212021534 | 2020-120 |
00815212021527 | 2020-100 |
00815212021510 | 2020-04 |
00815212021503 | 2020-03 |
00815212021497 | 2020-02 |
00815212021480 | 2020-01 |
00815212020469 | TS2090 |
00815212020452 | TS2005 |
00815212020445 | TS2004 |
00815212020438 | TS2003 |
00815212020421 | TS2002 |
00815212020414 | TS2001 |
00815212020407 | TS1010 |
00815212024436 | 2020-120-CAS |