Primary Device ID | 00845384008101 |
NIH Device Record Key | 91ccf351-19dc-4575-8194-72fe7d155430 |
Commercial Distribution Discontinuation | 2023-10-12 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | S-4DC |
Catalog Number | S-4DC |
Company DUNS | 079116867 |
Company Name | Anspach Effort, The |
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 | true |
OTC Over-The-Counter | false |
Phone | +1(800)255-2500 |
RA-DPYNA-anspachpowe@its.jnj.com | |
Phone | +1(800)255-2500 |
RA-DPYNA-anspachpowe@its.jnj.com | |
Phone | +1(800)255-2500 |
RA-DPYNA-anspachpowe@its.jnj.com | |
Phone | +1(800)255-2500 |
RA-DPYNA-anspachpowe@its.jnj.com | |
Phone | +1(800)255-2500 |
RA-DPYNA-anspachpowe@its.jnj.com | |
Phone | +1(800)255-2500 |
RA-DPYNA-anspachpowe@its.jnj.com | |
Phone | +1(800)255-2500 |
RA-DPYNA-anspachpowe@its.jnj.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00845384008101 [Primary] |
ERL | DRILL, SURGICAL, ENT (ELECTRIC OR PNEUMATIC) INCLUDING HANDPIECE |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-10-19 |
Device Publish Date | 2016-09-09 |
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00845384018537 - KINCISE™ | 2020-05-06 KINCISE RECHARGEABLE LI-ION BATTERY |
00845384018544 - KINCISE™ | 2020-05-06 KINCISE 4-PORT BATTERY CHARGER |
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00845384018568 - KINCISE™ | 2020-05-06 KINCISE ANTERIOR BROACH ADAPTER |