Primary Device ID | 06912547394952 |
NIH Device Record Key | cde797d0-8720-46df-81c3-862c012e10c2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Open Lateral Connector |
Version Model Number | 803835630 |
Company DUNS | 545249039 |
Company Name | Shandong Weigao Orthopaedic Device Co., Ltd. |
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 | true |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | true |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06912547394952 [Primary] |
KWP | Appliance, Fixation, Spinal Interlaminal |
Steralize Prior To Use | true |
Device Is Sterile | false |
[06912547394952]
Moist Heat or Steam Sterilization
[06912547394952]
Moist Heat or Steam Sterilization
[06912547394952]
Moist Heat or Steam Sterilization
[06912547394952]
Moist Heat or Steam Sterilization
[06912547394952]
Moist Heat or Steam Sterilization
[06912547394952]
Moist Heat or Steam Sterilization
[06912547394952]
Moist Heat or Steam Sterilization
[06912547394952]
Moist Heat or Steam Sterilization
[06912547394952]
Moist Heat or Steam Sterilization
[06912547394952]
Moist Heat or Steam Sterilization
[06912547394952]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-12-12 |
06912547394983 | 803835660 |
06912547394976 | 803835650 |
06912547394969 | 803835640 |
06912547394952 | 803835630 |
06912547394945 | 803835625 |
06912547394938 | 803835620 |
06912547394921 | 803835615 |