Primary Device ID | 00863634000408 |
NIH Device Record Key | 38ab2e90-e571-41f3-a755-70f58add04c8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SECQURE Ultimate |
Version Model Number | CQ5560ULT |
Company DUNS | 079554198 |
Company Name | SECQURE SURGICAL, CORP. |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00863634000408 [Primary] |
HET | Laparoscope, Gynecologic (And Accessories) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-01-09 |
Device Publish Date | 2017-09-19 |
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