| Primary Device ID | 05060940379425 |
| NIH Device Record Key | 1e275d1b-7a97-4c10-9e24-6fc3f9a21e21 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VaryFlex Glide, VFG, 21mm |
| Version Model Number | VFG21 |
| Company DUNS | 224419290 |
| Company Name | ENDOPERFECTION LIMITED |
| 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 | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05060940379425 [Primary] |
| EKS | File, Pulp Canal, Endodontic |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-06-27 |
| Device Publish Date | 2025-06-19 |
| 05060940379425 - VaryFlex Glide, VFG, 21mm | 2025-06-27 |
| 05060940379425 - VaryFlex Glide, VFG, 21mm | 2025-06-27 |
| 05060940379432 - VaryFlex Glide, VFG, 31mm | 2025-06-27 |
| 05060940379449 - VaryFlex Flow, VFF 21mm Size 45/04 | 2025-06-27 |
| 05060940379456 - VaryFlex Flow, VFF 21mm Size 50/04 | 2025-06-27 |
| 05060940379463 - VaryFlex Flow, VFF 25mm Size 45/04 | 2025-06-27 |
| 05060940379470 - VaryFlex Flow, VFF 25mm Size 50/04 | 2025-06-27 |
| 05060940379487 - VaryFlex Flow, VFF 31mm Size 45/04 | 2025-06-27 |
| 05060940379494 - VaryFlex Flow, VFF 31mm Size 50/04 | 2025-06-27 |