Primary Device ID | 00810125991509 |
NIH Device Record Key | 328679ac-f65d-4920-b931-a18b13290663 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ET RIGID LAB ANALOG |
Version Model Number | ETRLA540C |
Company DUNS | 796083090 |
Company Name | HIOSSEN, INC. |
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 | 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 | 00810125991509 [Primary] |
NDP | Accessories, Implant, Dental, Endosseous |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-07-11 |
Device Publish Date | 2024-07-03 |
00810019240706 | ETRLA7005S |
00810019240690 | ETRLA6007S |
00810019240683 | ETRLA6005S |
00810019240676 | ETRLA6004S |
00810019240669 | ETRLA5007S |
00810019240652 | ETRLA5005S |
00810019240645 | ETRLA5004S |
00810019240638 | ETRLA4507 |
00810019240621 | ETRLA4505 |
00810019240614 | ETRLA4504 |
00810019240607 | ETRLA4007 |
00810019240591 | ETRLA4005 |
00810019240584 | ETRLA4004 |
00810125991561 | ETRLA760C |
00810125991554 | ETRLA670C |
00810125991547 | ETRLA660C |
00810125991530 | ETRLA640C |
00810125991516 | ETRLA560C |
00810125991509 | ETRLA540C |
00810125991493 | ETRLA471C |
00810125991486 | ETRLA461C |
00810125991479 | ETRLA441C |
00810125991462 | ETRLA470C |
00810125991455 | ETRLA460C |
00810125991448 | ETRLA440C |
00810125991523 | ETRLA570C |