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 |