Primary Device ID | 04048844204099 |
NIH Device Record Key | b096fff0-3f67-4ef6-8054-75d4275252bc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | safety screw |
Version Model Number | 38200101 |
Company DUNS | 324369826 |
Company Name | implantcast GmbH |
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 Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04048844204099 [Primary] |
HSD | Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2025-06-09 |
Device Publish Date | 2020-11-18 |
04048844204099 - safety screw | 2025-06-09 |
04048844204099 - safety screw | 2025-06-09 |
04048844648336 - n/a | 2025-04-03 cancellous screw |
04048844648343 - n/a | 2025-04-03 cancellous screw |
04048844648350 - n/a | 2025-04-03 cancellous screw |
04048844648367 - n/a | 2025-04-03 cancellous screw |
04048844648374 - n/a | 2025-04-03 cancellous screw |
04048844065850 - AGILON® trial cap | 2025-03-18 |
04048844065867 - AGILON® trial cap | 2025-03-18 |