| Primary Device ID | 10709078012638 |
| NIH Device Record Key | 2c68d421-ab23-4222-9dc5-929aca7cd9c5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Tubing |
| Version Model Number | 0469 |
| 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 | 00709078012624 [Primary] |
| GS1 | 10709078012638 [Unit of Use] |
| OFP | Anesthesia Breathing Circuit Kit (Adult & Pediatric) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-05-27 |
| Device Publish Date | 2021-05-19 |
| 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 |