| Primary Device ID | 20857878007440 | 
| NIH Device Record Key | b97ae9dc-b799-4816-81cc-35145fccf0ca | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | BAN-11SF, F/G, STERILE | 
| Version Model Number | 11 Gauge x 13cm | 
| Catalog Number | BAN-11SF | 
| Company DUNS | 121622872 | 
| Company Name | RANFAC CORP. | 
| Device Count | 1 | 
| DM Exempt | false | 
| Pre-market Exempt | true | 
| 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 | true | 
| RX Perscription | true | 
| OTC Over-The-Counter | false | 
| Phone | 5085884400 | 
| info@ranfac.com | 
| Needle Gauge | 11 Gauge | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00857878007446 [Primary] | 
| GS1 | 10857878007443 [Package] Contains: 00857878007446 Package: Inner Pack [1 Units] In Commercial Distribution | 
| GS1 | 20857878007440 [Package] Contains: 10857878007443 Package: Case [10 Units] In Commercial Distribution | 
| OCJ | Spinal Channeling Instrument, Vertebroplasty | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2019-11-25 | 
| Device Publish Date | 2019-11-15 | 
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