HS Fiber
GUDID 20810020082986
Suture
RIVERPOINT MEDICAL, LLC
Polyolefin suture, multifilament| Primary Device ID | 20810020082986 |
| NIH Device Record Key | bdb51bc4-f9c2-4db9-a54f-22969adc0f2a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | HS Fiber |
| Version Model Number | HS232 |
| Company DUNS | 964053560 |
| Company Name | RIVERPOINT MEDICAL, LLC |
| 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 | 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 | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810020082999 [Primary] |
| GS1 | 20810020082986 [Package] Contains: 00810020082999 Package: [12 Units] In Commercial Distribution |
FDA Product Code
| GAT | Suture, Nonabsorbable, Synthetic, Polyethylene |
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 | 2020-03-12 |
| Device Publish Date | 2020-03-04 |
On-Brand Devices [HS Fiber]
Trademark Results [HS Fiber]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 HS FIBER 85392505 4125447 Live/Registered |
RIVERPOINT MEDICAL, LLC 2011-08-08 |
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