T.A.G.
GUDID B504SR1100268840
Provision
Suturing unit, reprocessed| Primary Device ID | B504SR1100268840 |
| NIH Device Record Key | b7eef079-68c8-4a3c-9b53-e36c0580f714 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | T.A.G. |
| Version Model Number | 110026884 |
| Company DUNS | 016889401 |
| Company Name | Provision |
| Device Count | 1 |
| DM Exempt | true |
| 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 | 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 |
Customer Support Contacts
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com | |
| Phone | 541-480-7953 |
| customersupport@provisiondrs.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B504SR1100268840 [Primary] |
FDA Product Code
| HWQ | Passer |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-10-08 |
| Device Publish Date | 2024-09-30 |
Devices Manufactured by Provision
| B504OM722018110 - Smith and Nephew | 2024-11-11 |
| B504CT2055A10 - Stryker | 2024-11-04 |
| B504OM722050010 - Smith and Nephew | 2024-10-30 |
| B504ES62902080250 - Stryker | 2024-10-08 |
| B504GS12630 - Avalign | 2024-10-08 |
| B504GS3350L4G0 - Cooper Medical | 2024-10-08 |
| B504GS60450500 - Invotec | 2024-10-08 |
| B504OM0210004500 - Stryker | 2024-10-08 |
Trademark Results [T.A.G.]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 T.A.G. 76551725 not registered Dead/Abandoned |
Aristocrat Technologies Australia Pty Ltd 2003-10-10 |
 T.A.G. 75204710 not registered Dead/Abandoned |
Digital Renaissance Inc. 1996-11-26 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.