| Primary Device ID | 00685447002055 | 
| NIH Device Record Key | b6cce3fd-d36c-463c-8dd5-3e7789d871e4 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Anchor 90 Deg Ball Probe, 1.7 mm Dia | 
| Version Model Number | PSZ-400-300 | 
| Company DUNS | 249225954 | 
| Company Name | Baylis Médicale Cie Inc | 
| Device Count | 1 | 
| DM Exempt | false | 
| Pre-market Exempt | false | 
| MRI Safety Status | MR Unsafe | 
| 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 | 00685447002055 [Primary] | 
| HRX | Arthroscope | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 3 | 
| Public Version Date | 2018-07-06 | 
| Device Publish Date | 2017-06-16 | 
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