| Primary Device ID | 07610221010370 | 
| NIH Device Record Key | 2ef4a524-1d3f-47b0-afce-c83d58fbcfde | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Geistlich Combi-Kit Collagen | 
| Version Model Number | 20146 | 
| Company DUNS | 480781728 | 
| Company Name | Geistlich Pharma AG | 
| 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 | true | 
| 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 | 07610221010370 [Primary] | 
| NPL | Barrier, Animal Source, Intraoral | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 3 | 
| Public Version Date | 2018-08-09 | 
| Device Publish Date | 2015-09-01 | 
| 07610221010141 - SwissGraft X D-Line | 2025-08-11 | 
| 07610221010158 - SwissGraft X D-Line | 2025-08-11 | 
| 07610221010219 - SwissMembrane X D-Line | 2025-08-11 | 
| 07610221010257 - SwissMembrane X D-Line | 2025-08-11 | 
| 07610221015375 - SwissGraft X D-Line | 2025-08-11 | 
| 07610221015382 - SwissGraft X D-Line | 2025-08-11 | 
| 07610221015429 - SwissMembrane X D-Line | 2025-08-11 | 
| 07610221016020 - Geistlich Bio-Oss® Flow | 2025-07-09 |