Primary Device ID | 00814008022922 |
NIH Device Record Key | f407284f-aad9-40a5-9a56-a151b6e27fbe |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | nvc |
Version Model Number | AC-1214T-401 |
Company DUNS | 047486041 |
Company Name | NVISION BIOMEDICAL TECHNOLOGIES, INC. |
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 | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | 210-545-3713 |
diana@nvisionbiomed.com | |
Phone | 210-545-3713 |
diana@nvisionbiomed.com | |
Phone | 210-545-3713 |
diana@nvisionbiomed.com | |
Phone | 210-545-3713 |
diana@nvisionbiomed.com | |
Phone | 210-545-3713 |
diana@nvisionbiomed.com | |
Phone | 210-545-3713 |
diana@nvisionbiomed.com | |
Phone | 210-545-3713 |
diana@nvisionbiomed.com | |
Phone | 210-545-3713 |
diana@nvisionbiomed.com | |
Phone | 210-545-3713 |
diana@nvisionbiomed.com |
Angle | 0 degree |
Angle | 0 degree |
Angle | 0 degree |
Angle | 0 degree |
Angle | 0 degree |
Angle | 0 degree |
Angle | 0 degree |
Angle | 0 degree |
Height | 6 Millimeter |
Length | 12 Millimeter |
Width | 14 Millimeter |
Angle | 0 degree |
Height | 6 Millimeter |
Length | 12 Millimeter |
Width | 14 Millimeter |
Angle | 0 degree |
Height | 6 Millimeter |
Length | 12 Millimeter |
Width | 14 Millimeter |
Angle | 0 degree |
Height | 6 Millimeter |
Length | 12 Millimeter |
Width | 14 Millimeter |
Angle | 0 degree |
Height | 6 Millimeter |
Length | 12 Millimeter |
Width | 14 Millimeter |
Angle | 0 degree |
Height | 6 Millimeter |
Length | 12 Millimeter |
Width | 14 Millimeter |
Angle | 0 degree |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00814008022922 [Primary] |
HTR | Rasp |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00814008022922]
Moist Heat or Steam Sterilization
[00814008022922]
Moist Heat or Steam Sterilization
[00814008022922]
Moist Heat or Steam Sterilization
[00814008022922]
Moist Heat or Steam Sterilization
[00814008022922]
Moist Heat or Steam Sterilization
[00814008022922]
Moist Heat or Steam Sterilization
[00814008022922]
Moist Heat or Steam Sterilization
[00814008022922]
Moist Heat or Steam Sterilization
[00814008022922]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2020-01-20 |
Device Publish Date | 2016-05-30 |
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00814008023127 | Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) |
00814008023110 | Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) |
00814008023103 | Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) |
00814008023097 | Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) |
00814008023080 | Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) |
00814008023073 | Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) |
00814008023066 | Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) |
00814008023059 | Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) |
00814008023042 | Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) |
00814008023035 | Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) |
00814008023028 | Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) |
00814008023011 | Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) |
00814008023004 | Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) |
00814008022991 | Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) |
00814008022984 | Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) |
00814008022977 | Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) |
00814008022960 | Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) |
00814008022953 | Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) |
00814008022946 | Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) |
00814008022939 | Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) |
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00814008022915 | Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) |
00814008022908 | Instrument, Trial, Anterior Cervical Interbody Fusion System (ACIF) |
00814008022892 | Instrument, Trial, Anterior Cervical Interbody Fusion System (ACIF) |
00814008022885 | Instrument, Trial, Anterior Cervical Interbody Fusion System (ACIF) |
00814008022878 | Instrument, Trial, Anterior Cervical Interbody Fusion System (ACIF) |
00814008022861 | Instrument, Trial, Anterior Cervical Interbody Fusion System (ACIF) |
00814008022854 | Instrument, Trial, Anterior Cervical Interbody Fusion System (ACIF) |
00814008022847 | Instrument, Trial, Anterior Cervical Interbody Fusion System (ACIF) |
00814008022830 | Instrument, Trial, Anterior Cervical Interbody Fusion System (ACIF) |
00814008022823 | Instrument, Trial, Anterior Cervical Interbody Fusion System (ACIF) |
00814008022816 | Instrument, Trial, Anterior Cervical Interbody Fusion System (ACIF) |
00814008022809 | Instrument, Trial, Anterior Cervical Interbody Fusion System (ACIF) |
00814008022793 | Instrument, Trial, Anterior Cervical Interbody Fusion System (ACIF) |
00814008022786 | Instrument, Trial, Anterior Cervical Interbody Fusion System (ACIF) |