Primary Device ID | 10871321001208 |
NIH Device Record Key | e457fc26-d3f2-42d1-8dab-e06b7be5e843 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Oval Sponge |
Version Model Number | S 1981-7.5 |
Company DUNS | 248911026 |
Company Name | Labtician Ophthalmics, Inc |
Device Count | 5 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 | 00871321000044 [Unit of Use] |
GS1 | 10871321001208 [Primary] |
HQX | Implant, Orbital, Extra-Ocular |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2021-01-27 |
Device Publish Date | 2018-02-22 |
18713210001192 | S 1981-7 |
18713210001185 | S 1981-5 |
18713210001178 | S 1981-4 |
18713210001208 | Oval Sponge |
10871321001208 | Oval Sponge |
10871321001192 | S 1981-7 |
10871321001185 | S 1981-5 |
10871321001178 | S 1981-4 |