E.M. Adams Co Inc

GUDID 50840200325580

SUTURE REMOVAL TRAY

E.M. ADAMS, INC.

Suture removal kit Suture removal kit Suture removal kit Suture removal kit Suture removal kit Suture removal kit Suture removal kit Suture removal kit Suture removal kit Suture removal kit Suture removal kit Suture removal kit Suture removal kit Suture removal kit Suture removal kit Suture removal kit Suture removal kit
Primary Device ID50840200325580
NIH Device Record Keyf8c66358-57b8-40ec-bd9a-0ccdf18760ee
Commercial Distribution StatusIn Commercial Distribution
Brand NameE.M. Adams Co Inc
Version Model Number14-70809JK-1
Company DUNS001403807
Company NameE.M. ADAMS, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(772)461-0532
EmailEMADAMS@EMADAMSCO.COM
Phone+1(772)461-0532
EmailEMADAMS@EMADAMSCO.COM
Phone+1(772)461-0532
EmailEMADAMS@EMADAMSCO.COM
Phone+1(772)461-0532
EmailEMADAMS@EMADAMSCO.COM
Phone+1(772)461-0532
EmailEMADAMS@EMADAMSCO.COM
Phone+1(772)461-0532
EmailEMADAMS@EMADAMSCO.COM
Phone+1(772)461-0532
EmailEMADAMS@EMADAMSCO.COM
Phone+1(772)461-0532
EmailEMADAMS@EMADAMSCO.COM
Phone+1(772)461-0532
EmailEMADAMS@EMADAMSCO.COM
Phone+1(772)461-0532
EmailEMADAMS@EMADAMSCO.COM
Phone+1(772)461-0532
EmailEMADAMS@EMADAMSCO.COM
Phone+1(772)461-0532
EmailEMADAMS@EMADAMSCO.COM
Phone+1(772)461-0532
EmailEMADAMS@EMADAMSCO.COM
Phone+1(772)461-0532
EmailEMADAMS@EMADAMSCO.COM
Phone+1(772)461-0532
EmailEMADAMS@EMADAMSCO.COM
Phone+1(772)461-0532
EmailEMADAMS@EMADAMSCO.COM
Phone+1(772)461-0532
EmailEMADAMS@EMADAMSCO.COM

Device Dimensions

Device Size Text, specify0
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Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS110840200325599 [Primary]
GS150840200325580 [Package]
Contains: 10840200325599
Package: Case [100 Units]
In Commercial Distribution

FDA Product Code

MCZSuture Removal Kit

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[50840200325580]

Ethylene Oxide


[50840200325580]

Ethylene Oxide


[50840200325580]

Ethylene Oxide


[50840200325580]

Ethylene Oxide


[50840200325580]

Ethylene Oxide


[50840200325580]

Ethylene Oxide


[50840200325580]

Ethylene Oxide


[50840200325580]

Ethylene Oxide


[50840200325580]

Ethylene Oxide


[50840200325580]

Ethylene Oxide


[50840200325580]

Ethylene Oxide


[50840200325580]

Ethylene Oxide


[50840200325580]

Ethylene Oxide


[50840200325580]

Ethylene Oxide


[50840200325580]

Ethylene Oxide


[50840200325580]

Ethylene Oxide


[50840200325580]

Ethylene Oxide


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-11-29
Device Publish Date2023-11-21

On-Brand Devices [E.M. Adams Co Inc]

10840200325551LACERATION TRAY
50840200301072LACERATION TRAY
50840200325580SUTURE REMOVAL TRAY

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