Primary Device ID | 00814913025674 |
NIH Device Record Key | a95c1a8d-4913-4a6b-9f36-51d6eaa1a006 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ET PICK-UP GUIDE PIN |
Version Model Number | ETFPG10ML |
Company DUNS | 796083090 |
Company Name | HIOSSEN, 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 | true |
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 | 00814913025674 [Primary] |
NDP | Accessories, Implant, Dental, Endosseous |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-12-07 |
Device Publish Date | 2018-09-11 |
00814913025728 | ETFPG10SL |
00814913025711 | ETFPG05SL |
00814913025704 | ETFPG05S |
00814913025698 | ETFPG00SL |
00814913025681 | ETFPG00S |
00814913025674 | ETFPG10ML |
00814913025667 | ETFPG05ML |
00814913025650 | ETFPG05M |
00814913025643 | ETFPG00ML |
00814913025636 | ETFPG00M |
00810125995019 | ETPGPR200LC |
00810125995002 | ETPGPR150LC |
00810125994999 | ETPGPR150C |
00810125994982 | ETPGPR100LC |
00810125994975 | ETPGPR100C |
00810125994968 | ETPGPM200LC |
00810125994951 | ETPGPM150LC |
00810125994944 | ETPGPM150C |
00810125994937 | ETPGPM100LC |
00810125994920 | ETPGPM100C |