Primary Device ID | 20811955020715 |
NIH Device Record Key | f4df2b05-0d3a-4361-8bfe-844b51dced97 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | OverStitch Endoscopic Suturing System Sx |
Version Model Number | ESS-G02-Sx1 |
Catalog Number | ESS-G02-Sx1 |
Company DUNS | 625064352 |
Company Name | Apollo Endosurgery, Inc. |
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 | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | true |
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 | 10811955020718 [Primary] |
GS1 | 20811955020715 [Package] Contains: 10811955020718 Package: Case [3 Units] In Commercial Distribution |
HCF | Instrument, Ligature Passing And Knot Tying |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-06-03 |
Device Publish Date | 2021-05-26 |
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