| Primary Device ID | 06975222391035 | 
| NIH Device Record Key | 1a1655d7-d486-466b-a9d1-1b84608a32ea | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | SpinMedix® Absorbable Fibrous Membrane | 
| Version Model Number | ZK-004 | 
| 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 | 06975222391035 [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 |