Primary Device ID | 25056030400135 |
NIH Device Record Key | 6e603bb0-761c-41a8-9360-c997a656bd51 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Anaesthetic Needles |
Version Model Number | M0638-02/10 |
Catalog Number | M0638 |
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 | 25056030400135 [Unit of Use] |
GS1 | 35056030400132 [Primary] |
MED | Sterilant, Medical Devices |
Steralize Prior To Use | true |
Device Is Sterile | true |
[25056030400135]
Ethylene Oxide
[25056030400135]
Ethylene Oxide
[25056030400135]
Ethylene Oxide
[25056030400135]
Ethylene Oxide
[25056030400135]
Ethylene Oxide
[25056030400135]
Ethylene Oxide
[25056030400135]
Ethylene Oxide
[25056030400135]
Ethylene Oxide
[25056030400135]
Ethylene Oxide
[25056030400135]
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 |