Primary Device ID | 00802357132805 |
NIH Device Record Key | 24fd0b43-1d38-4ebe-be37-702fa3a00f49 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Prosplints |
Version Model Number | 113280 |
Company DUNS | 003173028 |
Company Name | MEDICAL SPECIALTIES INCORPORATED |
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 | false |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00802357132805 [Primary] |
IQI | Orthosis, Limb Brace |
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 |
00802357137442 | 113744 |
00802357137435 | 113743 |
00802357137411 | 113741 |
00802357132805 | 113280 |
00802357130719 | 113071 |
00802357130702 | 113070 |
00802357130542 | 113054 |
00802357130528 | 113052 |
00802357130511 | 113051 |
00802357130344 | 113034 |
00802357130320 | 113032 |
00802357130313 | 113031 |
00802357130115 | 113011 |
00802357130108 | 113010 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() PROSPLINTS 73267898 1180983 Live/Registered |
Medical Specialties Incorporated 1980-06-26 |