| Primary Device ID | 06975222391059 |
| NIH Device Record Key | 93d43143-9854-4862-9617-cbdc41a91d07 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SpinMedix® Absorbable Fibrous Membrane |
| Version Model Number | ZK-006 |
| Company DUNS | 702939498 |
| Company Name | Ningbo Guangyuan Zhixin Biological Technology Co., Ltd. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | true |
| Manufacturing Date | true |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 06975222391059 [Primary] |
| OWW | Mesh, Surgical, Absorbable, Orthopaedics, Reinforcement Of Tendon |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-05-28 |
| Device Publish Date | 2025-05-20 |
| 06975222391196 | ZK-020 |
| 06975222391189 | ZK-019 |
| 06975222391172 | ZK-018 |
| 06975222391165 | ZK-017 |
| 06975222391158 | ZK-016 |
| 06975222391141 | ZK-015 |
| 06975222391134 | ZK-014 |
| 06975222391127 | ZK-013 |
| 06975222391110 | ZK-012 |
| 06975222391103 | ZK-011 |
| 06975222391097 | ZK-010 |
| 06975222391080 | ZK-009 |
| 06975222391073 | ZK-008 |
| 06975222391066 | ZK-007 |
| 06975222391059 | ZK-006 |
| 06975222391042 | ZK-005 |
| 06975222391035 | ZK-004 |
| 06975222391028 | ZK-003 |
| 06975222391011 | ZK-002 |
| 06975222391004 | ZK-001 |