Primary Device ID | 00810006682502 |
NIH Device Record Key | cba97dec-c692-4d7d-a210-64d4c5a85ecc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Wrist Drop w/ U-Cuff Hand Splint |
Version Model Number | WDS01RL |
Catalog Number | WDS01RL |
Company DUNS | 958758146 |
Company Name | PRIMO INC |
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 | 00810006682502 [Primary] |
ILH | Splint, Hand, And Components |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-03-11 |
Device Publish Date | 2019-02-27 |
00810006682533 | Wrist Drop w/ U-Cuff Hand Splint - XLarge (Right) |
00810006682526 | Wrist Drop w/ U-Cuff Hand Splint - Small (Right) |
00810006682519 | Wrist Drop w/ U-Cuff Hand Splint - Medium (Right) |
00810006682502 | Wrist Drop w/ U-Cuff Hand Splint - Large (Right) |
00810006682496 | Wrist Drop w/ U-Cuff Hand Splint - XLarge (Left) |
00810006682489 | Wrist Drop w/ U-Cuff Hand Splint - Small (Left) |
00810006682472 | Wrist Drop w/ U-Cuff Hand Splint - Medium (Left) |
00810006682465 | Wrist Drop w/ U-Cuff Hand Splint - Large (Left) |