| Primary Device ID | 45056030400870 |
| NIH Device Record Key | 95729e8b-3e3c-49f4-b341-b579958589a4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Refractive Cannulae |
| Version Model Number | M3914-02/10 |
| Catalog Number | M3914 |
| Company DUNS | 504799313 |
| Company Name | STERIMEDIX LIMITED |
| Device Count | 10 |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 15056030400879 [Primary] |
| GS1 | 45056030400870 [Unit of Use] |
| MED | Sterilant, Medical Devices |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[45056030400870]
Ethylene Oxide
[45056030400870]
Ethylene Oxide
[45056030400870]
Ethylene Oxide
[45056030400870]
Ethylene Oxide
[45056030400870]
Ethylene Oxide
[45056030400870]
Ethylene Oxide
[45056030400870]
Ethylene Oxide
[45056030400870]
Ethylene Oxide
[45056030400870]
Ethylene Oxide
[45056030400870]
Ethylene Oxide
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-10-15 |
| Device Publish Date | 2024-10-07 |
| 35056030400422 | 25g x 7/8" Lin Lasik |
| 15056030400428 | 25g x 7/8" Lin Lasik |
| 25056030400999 | 25g x 7/8" Lin Lasik |
| 25056030400449 | 25g x 7/8" Lasik Irrig |
| 45056030400870 | 23g x 22mm LASIK Irr |
| 35056030400484 | 26g x 7/8" LASIK Slade |
| 45056030400436 | 25g x 1 1/8" Buratto Lasi |