Primary Device ID | 00817708022988 |
NIH Device Record Key | 57f890f6-807c-4e97-ab0d-7dd4cd84d403 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AccuSert |
Version Model Number | FP-0010080 |
Company DUNS | 622637544 |
Company Name | EMED TECHNOLOGIES CORPORATION |
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 | 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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817708022988 [Primary] |
KZH | Introducer, Syringe Needle |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-11-01 |
Device Publish Date | 2022-10-24 |
00817708022988 | SAF-SUB-Q Needle Inserter |
00817708022964 | OPTFlow Needle Inserter |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() ACCUSERT 88156696 not registered Live/Pending |
EMED TECHNOLOGIES CORPORATION 2018-10-16 |
![]() ACCUSERT 73698886 1500988 Dead/Cancelled |
EMHART INDUSTRIES, INC. 1987-11-30 |
![]() ACCUSERT 73583681 1437187 Dead/Cancelled |
CILCO, INC. 1986-02-19 |