Ellis Instruments, Inc.

GUDID 00860007290664

Ellis Instruments Inc

Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps
Primary Device ID00860007290664
NIH Device Record Key6bf985c0-baa1-4705-abbb-8ebca7f835de
Commercial Distribution StatusIn Commercial Distribution
Brand NameEllis Instruments, Inc.
Version Model Number#125-815
Company DUNS926867201
Company NameEllis Instruments Inc
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100860007290664 [Primary]

FDA Product Code

GENForceps, General & Plastic Surgery

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[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


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-11-15
Device Publish Date2021-11-05

On-Brand Devices [Ellis Instruments, Inc. ]

00860007290664#125-815
00860007290640#125-080
00860007290626#125-025
00860007290602#125-024

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.