Primary Device ID | 17310231150048 |
NIH Device Record Key | f2879451-cbaa-4372-b028-53df611ca31a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PractiPal |
Version Model Number | Foam Large |
Catalog Number | 115004 |
Company DUNS | 353954381 |
Company Name | Directa AB |
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 | true |
Expiration Date | false |
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 | 17310231150048 [Primary] |
FSM | Tray, Surgical, Instrument |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-12-15 |
Device Publish Date | 2022-12-07 |
17310231151205 | Clips |
17310231150048 | Foam Large |
17310231150031 | Foam |
17310231150024 | Waste Cup |
17310231150017 | MultiPoint |
17310231150000 | MultiDappen |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PRACTIPAL 79017852 3225274 Live/Registered |
Directa AB 2005-08-17 |
PRACTIPAL 76215465 2757970 Dead/Cancelled |
ADELS, VERENA 2001-02-23 |
PRACTIPAL 76215465 2757970 Dead/Cancelled |
LIMMER, HELMUT 2001-02-23 |