Primary Device ID | 06975222391127 |
NIH Device Record Key | 73a09ade-fdec-46d3-88b0-c097d114a166 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SpinMedix® Absorbable Fibrous Membrane |
Version Model Number | ZK-013 |
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 | 06975222391127 [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 |