| Primary Device ID | 50560304001790 |
| NIH Device Record Key | 1e355232-1c73-4065-8212-c442a0b79865 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Anaesthetic Needles |
| Version Model Number | 0642A-03/Y |
| Catalog Number | M0642A |
| Company DUNS | 504799313 |
| Company Name | STERIMEDIX 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 | 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 | 50560304001790 [Primary] |
| MED | Sterilant, Medical Devices |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[50560304001790]
Ethylene Oxide
[50560304001790]
Ethylene Oxide
[50560304001790]
Ethylene Oxide
[50560304001790]
Ethylene Oxide
[50560304001790]
Ethylene Oxide
[50560304001790]
Ethylene Oxide
[50560304001790]
Ethylene Oxide
[50560304001790]
Ethylene Oxide
[50560304001790]
Ethylene Oxide
[50560304001790]
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 |
| 50560304001790 | 25g x 7/8" Peribulbar |
| 50560304001240 | 23g x 1 1/2" Retrobulbar |
| 50560304000250 | 25g x 1 1/2" Retrobulbar |
| 25056030400180 | 23g x 1 1/4" Peribulbar |
| 25056030400166 | 25g x 1 1/4" Peribulbar |
| 25056030400135 | 23g x 1 1/2" Retrobulbar |
| 25056030400128 | 25g x 1 1/2" Retrobulbar |
| 05056030403972 | 19g x 1" Sub Tenon |
| 05056030400186 | 23g x 1 1/4" Peribulbar |
| 05056030400162 | 25g x 1 1/4" Peribulbar |