Primary Device ID | 04719872920380 |
NIH Device Record Key | 4f557e50-b039-4053-9a04-fa0834ce73e2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cross-Seal |
Version Model Number | 002 |
Catalog Number | 002 |
Company DUNS | 656078460 |
Company Name | MEDEON BIODESIGN, 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 | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04719872920380 [Primary] |
GS1 | 04719872920397 [Package] Package: Box [1 Units] In Commercial Distribution |
GS1 | 04719872920403 [Package] Contains: 04719872920397 Package: Carton [12 Units] In Commercial Distribution |
MGB | Device, Hemostasis, Vascular |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-02-09 |
Device Publish Date | 2022-02-01 |
04719872920380 | The Cross-Seal Accessories (Cross-Seal Knot Tyer, Cross-Seal Knot Pusher, and Cross-Seal Suture |
04719872920359 | The Cross-Seal Device is composed of a Catheter, Suture Delivery System, and Handle. The Cross-S |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CROSS-SEAL 88046024 not registered Live/Pending |
Terumo Kabushiki Kaisha 2018-07-20 |
CROSS-SEAL 86940340 not registered Dead/Abandoned |
SPC Resources, Inc. 2016-03-15 |