Primary Device ID | 00860007290664 |
NIH Device Record Key | 6bf985c0-baa1-4705-abbb-8ebca7f835de |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ellis Instruments, Inc. |
Version Model Number | #125-815 |
Company DUNS | 926867201 |
Company Name | Ellis Instruments 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 | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
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 | 00860007290664 [Primary] |
GEN | Forceps, General & Plastic Surgery |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00860007290664]
Moist Heat or Steam Sterilization
[00860007290664]
Moist Heat or Steam Sterilization
[00860007290664]
Moist Heat or Steam Sterilization
[00860007290664]
Moist Heat or Steam Sterilization
[00860007290664]
Moist Heat or Steam Sterilization
[00860007290664]
Moist Heat or Steam Sterilization
[00860007290664]
Moist Heat or Steam Sterilization
[00860007290664]
Moist Heat or Steam Sterilization
[00860007290664]
Moist Heat or Steam Sterilization
[00860007290664]
Moist Heat or Steam Sterilization
[00860007290664]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-11-15 |
Device Publish Date | 2021-11-05 |
00860007290664 | #125-815 |
00860007290640 | #125-080 |
00860007290626 | #125-025 |
00860007290602 | #125-024 |