Primary Device ID | 00813110028990 |
NIH Device Record Key | c81c441e-8b9c-44f7-9af3-8d5843b6b995 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Instrument |
Version Model Number | 260-101-026 |
Catalog Number | 260-101-026 |
Company DUNS | 945015758 |
Company Name | BICON, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 617-524-4443 |
support@bicon.com | |
Phone | 617-524-4443 |
support@bicon.com | |
Phone | 617-524-4443 |
support@bicon.com | |
Phone | 617-524-4443 |
support@bicon.com | |
Phone | 617-524-4443 |
support@bicon.com | |
Phone | 617-524-4443 |
support@bicon.com | |
Phone | 617-524-4443 |
support@bicon.com | |
Phone | 617-524-4443 |
support@bicon.com | |
Phone | 617-524-4443 |
support@bicon.com | |
Phone | 617-524-4443 |
support@bicon.com | |
Phone | 617-524-4443 |
support@bicon.com | |
Phone | 617-524-4443 |
support@bicon.com | |
Phone | 617-524-4443 |
support@bicon.com | |
Phone | 617-524-4443 |
support@bicon.com | |
Phone | 617-524-4443 |
support@bicon.com | |
Phone | 617-524-4443 |
support@bicon.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00813110028990 [Primary] |
DZN | Instruments, Dental Hand |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00813110028990]
Moist Heat or Steam Sterilization
[00813110028990]
Moist Heat or Steam Sterilization
[00813110028990]
Moist Heat or Steam Sterilization
[00813110028990]
Moist Heat or Steam Sterilization
[00813110028990]
Moist Heat or Steam Sterilization
[00813110028990]
Moist Heat or Steam Sterilization
[00813110028990]
Moist Heat or Steam Sterilization
[00813110028990]
Moist Heat or Steam Sterilization
[00813110028990]
Moist Heat or Steam Sterilization
[00813110028990]
Moist Heat or Steam Sterilization
[00813110028990]
Moist Heat or Steam Sterilization
[00813110028990]
Moist Heat or Steam Sterilization
[00813110028990]
Moist Heat or Steam Sterilization
[00813110028990]
Moist Heat or Steam Sterilization
[00813110028990]
Moist Heat or Steam Sterilization
[00813110028990]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-06-01 |
Device Publish Date | 2021-05-24 |
00813110027399 | Attachment Gauge |
00813110024619 | Straight Stealth Latch Driver |
00813110023957 | Hex Screwdriver |
00813110023902 | Reamer Removal Wrench |
00813110028990 | Hex Screwdriver, 20mm |
00813110028556 | FDUA Latch Driver |
00813110029539 | Mesh Screwdriver |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
INSTRUMENT 86648787 not registered Dead/Abandoned |
Wright, Bruce David 2015-06-02 |
INSTRUMENT 86251255 4640905 Live/Registered |
INSTRUMENT LLC 2014-04-14 |
INSTRUMENT 85068560 not registered Dead/Abandoned |
Instrument Skateboards LLC 2010-06-22 |
INSTRUMENT 77742928 3725465 Dead/Cancelled |
Instrument Marketing, Inc. 2009-05-22 |
INSTRUMENT 74508227 not registered Dead/Abandoned |
Pro Golf of America, Inc. 1994-04-04 |