E.M. Adams Co Inc

GUDID 10840200325551

LACERATION TRAY

E.M. ADAMS, INC.

Suture kit, non-medicated

• Primary Device ID: 10840200325551
• NIH Device Record Key: e4e290cb-125a-4646-ab3f-40ab4fbda8b6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: E.M. Adams Co Inc
• Version Model Number: 114-31613-1
• 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

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 Identifiers

Device Issuing Agency	Device ID
GS1	10840200325551 [Primary]
GS1	50840200325542 [Package]; Package: Case [20 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K812133

FDA Product Code

• FSM: Tray, Surgical, Instrument

Sterilization

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

[10840200325551]

Ethylene Oxide

[10840200325551]

Ethylene Oxide

[10840200325551]

Ethylene Oxide

[10840200325551]

Ethylene Oxide

[10840200325551]

Ethylene Oxide

[10840200325551]

Ethylene Oxide

[10840200325551]

Ethylene Oxide

[10840200325551]

Ethylene Oxide

[10840200325551]

Ethylene Oxide

[10840200325551]

Ethylene Oxide

[10840200325551]

Ethylene Oxide

[10840200325551]

Ethylene Oxide

[10840200325551]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-11-08
• Device Publish Date: 2023-10-31

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

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