Primary Device ID | 10709078011440 |
NIH Device Record Key | 6cd80ed8-af5c-4cd0-9c5c-b56a111db4bc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tubing |
Version Model Number | 2189 |
Company DUNS | 092673953 |
Company Name | WESTMED, INC. |
Device Count | 100 |
DM Exempt | false |
Pre-market Exempt | true |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00709078011436 [Primary] |
GS1 | 00709078012884 [Primary] |
GS1 | 10709078011440 [Unit of Use] |
BYX | Tubing, Pressure And Accessories |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-05-06 |
Device Publish Date | 2021-04-28 |
10709078011440 | Tubing, 10' KROT, W/Sleeves and Nuts, Vortran |
10709078011518 | Tubing, 20' KROT, Green, W/Sleeves and Nuts, Vortran |
10709078012638 | Tubing, Corrugate, Clear, 72" x 10mm |
10709078012652 | Tubing, Corrugate, 10mm x 1' Clear |
10709078012928 | Tubing, Corrugated 22mm X 120" |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() TUBING 98874040 not registered Live/Pending |
Blinc, Inc. 2024-11-26 |
![]() TUBING 73518151 not registered Dead/Abandoned |
S.A. HOLDITCH & ASSOCIATES, INC. 1985-01-18 |