Primary Device ID | 06009544000419 |
NIH Device Record Key | 72c6a97c-3a4f-4caa-8bad-09ff4cbc0a24 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | ABE10 |
Company DUNS | 636239584 |
Company Name | SOUTHERN IMPLANTS (PTY) LTD |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | 06009544000419 [Primary] |
FZE | Prosthesis, Nose, Internal |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2019-01-22 |
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