Primary Device ID | 25056030402542 |
NIH Device Record Key | ad61a3cb-3d57-454c-9fa3-4a6649b3a793 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Intradermal Cannulae |
Version Model Number | AE1711-02/40 |
Catalog Number | AE1711 |
Company DUNS | 504799313 |
Company Name | STERIMEDIX LIMITED |
Device Count | 40 |
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 | 15056030402545 [Primary] |
GS1 | 25056030402542 [Unit of Use] |
MED | Sterilant, Medical Devices |
Steralize Prior To Use | true |
Device Is Sterile | true |
[25056030402542]
Ethylene Oxide
[25056030402542]
Ethylene Oxide
[25056030402542]
Ethylene Oxide
[25056030402542]
Ethylene Oxide
[25056030402542]
Ethylene Oxide
[25056030402542]
Ethylene Oxide
[25056030402542]
Ethylene Oxide
[25056030402542]
Ethylene Oxide
[25056030402542]
Ethylene Oxide
[25056030402542]
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 |
25056030402535 | SILKANN CANNULA 18gx70mm |
25056030402245 | Intradermal Cannulae SILKANN CANNULA 18gx70mm |
15056030402651 | Silkann(FT)Cann 18gx70mm |
25056030402542 | SILKANN CANNULA 20g x60mm |