Primary Device ID | 00026072022771 |
NIH Device Record Key | daac3445-2d79-409e-b0ce-c2e9c39cec4a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SC |
Version Model Number | S500 |
Company DUNS | 119066872 |
Company Name | Allied Medical, LLC |
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 | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00026072022771 [Primary] |
FYH | Splint, Extremity, Noninflatable, External, Sterile |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-05-17 |
Device Publish Date | 2024-05-09 |
00026072022900 | 4 MINI SPLINT |
00026072022894 | 6 SPLINT KIT |
00026072022825 | ADULT HAND & WRIST |
00026072022818 | ADULT FULL LEG |
00026072022801 | ADULT 1/2 LEG |
00026072022795 | ADULT FULL ARM |
00026072022788 | ADULT 1/2 ARM |
00026072022771 | SPLINT KIT (% |
00026072012208 | ADULT FOOT AND ANKLE SPLINT |
00026072012215 | BLUE TIP TUBIN |