E.M. Adams Co Inc

GUDID 50840200325580

SUTURE REMOVAL TRAY

E.M. ADAMS, INC.

Suture removal kit

• Primary Device ID: 50840200325580
• NIH Device Record Key: f8c66358-57b8-40ec-bd9a-0ccdf18760ee
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: E.M. Adams Co Inc
• Version Model Number: 14-70809JK-1
• Company DUNS: 001403807
• Company Name: E.M. ADAMS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(772)461-0532
• Email: EMADAMS@EMADAMSCO.COM
• Phone: +1(772)461-0532
• Email: EMADAMS@EMADAMSCO.COM
• Phone: +1(772)461-0532
• Email: EMADAMS@EMADAMSCO.COM
• Phone: +1(772)461-0532
• Email: EMADAMS@EMADAMSCO.COM
• Phone: +1(772)461-0532
• Email: EMADAMS@EMADAMSCO.COM
• Phone: +1(772)461-0532
• Email: EMADAMS@EMADAMSCO.COM
• Phone: +1(772)461-0532
• Email: EMADAMS@EMADAMSCO.COM
• Phone: +1(772)461-0532
• Email: EMADAMS@EMADAMSCO.COM
• Phone: +1(772)461-0532
• Email: EMADAMS@EMADAMSCO.COM
• Phone: +1(772)461-0532
• Email: EMADAMS@EMADAMSCO.COM
• Phone: +1(772)461-0532
• Email: EMADAMS@EMADAMSCO.COM
• Phone: +1(772)461-0532
• Email: EMADAMS@EMADAMSCO.COM
• Phone: +1(772)461-0532
• Email: EMADAMS@EMADAMSCO.COM
• Phone: +1(772)461-0532
• Email: EMADAMS@EMADAMSCO.COM
• Phone: +1(772)461-0532
• Email: EMADAMS@EMADAMSCO.COM
• Phone: +1(772)461-0532
• Email: EMADAMS@EMADAMSCO.COM
• Phone: +1(772)461-0532
• Email: EMADAMS@EMADAMSCO.COM

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	10840200325599 [Primary]
GS1	50840200325580 [Package]; Contains: 10840200325599; Package: Case [100 Units]; In Commercial Distribution

FDA Product Code

• MCZ: Suture Removal Kit

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: true

[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 Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-11-29
• Device Publish Date: 2023-11-21

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

• 10840200325551: LACERATION TRAY
• 50840200301072: LACERATION TRAY
• 50840200325580: SUTURE REMOVAL TRAY