Count-Tainer 20

GUDID 00612376000135

ANCHOR PRODUCTS COMPANY

Sharps container Sharps container Sharps container Sharps container Sharps container Sharps container Sharps container Sharps container Sharps container Sharps container Sharps container Sharps container Sharps container Sharps container Sharps container Sharps container
Primary Device ID00612376000135
NIH Device Record Key99906b75-d8f5-469a-8f0f-6831ecd81f59
Commercial Distribution StatusIn Commercial Distribution
Brand NameCount-Tainer 20
Version Model Number5120FNS
Company DUNS005245386
Company NameANCHOR PRODUCTS COMPANY
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone800-323-5134
Emailinfo@anchorsurgical.com
Phone800-323-5134
Emailinfo@anchorsurgical.com
Phone800-323-5134
Emailinfo@anchorsurgical.com
Phone800-323-5134
Emailinfo@anchorsurgical.com
Phone800-323-5134
Emailinfo@anchorsurgical.com
Phone800-323-5134
Emailinfo@anchorsurgical.com
Phone800-323-5134
Emailinfo@anchorsurgical.com
Phone800-323-5134
Emailinfo@anchorsurgical.com
Phone800-323-5134
Emailinfo@anchorsurgical.com
Phone800-323-5134
Emailinfo@anchorsurgical.com
Phone800-323-5134
Emailinfo@anchorsurgical.com
Phone800-323-5134
Emailinfo@anchorsurgical.com
Phone800-323-5134
Emailinfo@anchorsurgical.com
Phone800-323-5134
Emailinfo@anchorsurgical.com
Phone800-323-5134
Emailinfo@anchorsurgical.com
Phone800-323-5134
Emailinfo@anchorsurgical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100612376000135 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MMKContainer, Sharps

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00612376000135]

Ethylene Oxide


[00612376000135]

Ethylene Oxide


[00612376000135]

Ethylene Oxide


[00612376000135]

Ethylene Oxide


[00612376000135]

Ethylene Oxide


[00612376000135]

Ethylene Oxide


[00612376000135]

Ethylene Oxide


[00612376000135]

Ethylene Oxide


[00612376000135]

Ethylene Oxide


[00612376000135]

Ethylene Oxide


[00612376000135]

Ethylene Oxide


[00612376000135]

Ethylene Oxide


[00612376000135]

Ethylene Oxide


[00612376000135]

Ethylene Oxide


[00612376000135]

Ethylene Oxide


[00612376000135]

Ethylene Oxide


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-19

On-Brand Devices [Count-Tainer 20]

006123760001355120FNS
106123760001015120F

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