| Primary Device ID | 04250203940696 |
| NIH Device Record Key | 8df9051a-d044-4627-b21b-9a87d84e2ca0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Access Kit |
| Version Model Number | US7ZA0000 |
| Company DUNS | 342087108 |
| Company Name | Joline GmbH & Co. KG |
| 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 |
|---|---|
| GS1 | 04250203940696 [Primary] |
| HRX | Arthroscope |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-08-24 |
| Device Publish Date | 2020-08-14 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ACCESS KIT 73617358 not registered Dead/Abandoned |
INTRA OPTICS LABORATORIES PTY. LIMITED 1986-08-29 |