USB Medical Delivery Foreceps DF-101

GUDID 00853512006790

HV Heart Retractor

NIKOMED USA

Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps Clamp manipulation forceps
Primary Device ID00853512006790
NIH Device Record Key7e45f55f-38d4-43db-a3e5-92c23ae381ba
Commercial Distribution StatusIn Commercial Distribution
Brand NameUSB Medical Delivery Foreceps
Version Model NumberDF-101
Catalog NumberDF-101
Company DUNS073648341
Company NameNIKOMED USA
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 Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100853512006790 [Primary]

FDA Product Code

GDJClamp, Surgical, General & Plastic Surgery

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00853512006790]

Moist Heat or Steam Sterilization


[00853512006790]

Moist Heat or Steam Sterilization


[00853512006790]

Moist Heat or Steam Sterilization


[00853512006790]

Moist Heat or Steam Sterilization


[00853512006790]

Moist Heat or Steam Sterilization


[00853512006790]

Moist Heat or Steam Sterilization


[00853512006790]

Moist Heat or Steam Sterilization


[00853512006790]

Moist Heat or Steam Sterilization


[00853512006790]

Moist Heat or Steam Sterilization


[00853512006790]

Moist Heat or Steam Sterilization


[00853512006790]

Moist Heat or Steam Sterilization


[00853512006790]

Moist Heat or Steam Sterilization


[00853512006790]

Moist Heat or Steam Sterilization


[00853512006790]

Moist Heat or Steam Sterilization


[00853512006790]

Moist Heat or Steam Sterilization


[00853512006790]

Moist Heat or Steam Sterilization


[00853512006790]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-03-21
Device Publish Date2023-03-13

Devices Manufactured by NIKOMED USA

00853512006806 - TRACE 12023-04-03 ECG Electrodes
00853512006783 - USB Medical HV Atrial Heart Retractor - Complete Set2023-03-21 HV Heart Retractor
00853512006790 - USB Medical Delivery Foreceps2023-03-21HV Heart Retractor
00853512006790 - USB Medical Delivery Foreceps2023-03-21 HV Heart Retractor
00853512006769 - NIKOPrep2022-10-27 Strips for Skin Preparation (1 card of 5 pieces)
00853512006776 - NIKOPrep2022-10-27 Strips for Skin Preparation (Individual Pieces)
00853512006752 - Nikotab2022-09-14 ECG Electrodes
20853512006640 - NikoSurg2022-02-03 Neutral Electrodes
00853512006745 - Nikomed ECG Cable2021-01-29 3 Lead Monitor Cable

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