| Primary Device ID | E203JCG60203 |
| NIH Device Record Key | b77a53d6-692f-4daf-b117-26acce7e2d7d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MONOGLYC |
| Version Model Number | MONOGLYC |
| Company DUNS | 341053195 |
| Company Name | Resorba Medical GmbH |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | E203JCG60203 [Primary] |
| GAM | Suture, Absorbable, Synthetic, Polyglycolic Acid |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-08-19 |
| Device Publish Date | 2021-08-11 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MONOGLYC 88350542 not registered Live/Pending |
CHOUKROUN, Joseph 2019-03-21 |