Primary Device ID | 10871321002571 |
NIH Device Record Key | 246e0e5f-9b07-4b54-bc69-5add6b7c4256 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Combo Pack |
Version Model Number | S 2083 |
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 | 00871321002567 [Unit of Use] |
GS1 | 10871321002571 [Primary] |
HQJ | Implant, Absorbable, (Scleral Buckling Methods) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2021-01-28 |
Device Publish Date | 2018-02-22 |
18713210002595 | Combo Pack |
18713210002571 | Combo Pack |
18713210002304 | Combo Pack |
18713210002106 | Combo Pack |
18713210002090 | Combo Pack |
18713210002069 | Combo Pack |
10871321002595 | Combo Pack |
10871321002571 | Combo Pack |
10871321002304 | Combo Pack |
10871321002106 | Combo Pack |
10871321002090 | Combo Pack |
10871321002069 | Combo Pack |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
COMBO PACK 78248710 3006422 Dead/Cancelled |
IDEAL Industries, Inc. 2003-05-12 |
COMBO PACK 75131009 2135313 Dead/Cancelled |
MACRO ENGINEERING & TECHNOLOGY INC. 1996-07-08 |
COMBO PACK 74273205 1748355 Dead/Cancelled |
PURE FILL CORPORATION 1992-05-05 |
COMBO PACK 73569063 1401012 Dead/Cancelled |
CAROUSEL INDUSTRIES, INC. 1985-11-18 |