| Primary Device ID | 08806388203512 | 
| NIH Device Record Key | b279c330-7904-45be-bf3e-7795378129c4 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Temporary Cylinder | 
| Version Model Number | AANOTCO6010 | 
| Catalog Number | AANOTCO6010T | 
| Company DUNS | 687388178 | 
| Company Name | Megagen Implant Co. Ltd | 
| 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 | true | 
| Manufacturing Date | true | 
| Expiration Date | false | 
| 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 | 08806388203512 [Primary] | 
| NHA | Abutment, Implant, Dental, Endosseous | 
| Steralize Prior To Use | true | 
| Device Is Sterile | false | 
[08806388203512]
Moist Heat or Steam Sterilization
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 5 | 
| Public Version Date | 2019-11-08 | 
| Device Publish Date | 2015-06-24 | 
| 08806388203512 | AnyRidge Internal Ø5.8/ Octa | 
| 08806388203505 | AnyRidge Internal Ø4.8/ Octa | 
| 08806388203499 | AnyRidge Internal Ø3.8/ Octa | 
| 08806388203482 | AnyRidge Internal Ø5.8/ Non-Octa | 
| 08806388203475 | AnyRidge Internal Ø4.8/ Non-Octa | 
| 08806388203468 | AnyRidge Internal Ø3.8/ Non-Octa | 
| 08806388244102 | Ø4.8 / L=10 | 
| 08809985656736 | Common | 
| 08809985656729 | Common | 
| 08809985656712 | Common | 
| 08809985653469 | Common | 
| 08809985653452 | Common | 
| 08809977450496 | Common | 
| 08809977450489 | Common | 
| 08809977450472 | Common | 
| 08809977450465 | Common | 
| 08809985666063 | Ø5/ H=4/ Single | 
| 08809985666001 | Ø5/ H=4/ Single |