Identification Labels 197823

GUDID 10886333208958

MLK Identification Labels with Marker

ARGON MEDICAL DEVICES, INC.

Procedural medication labelling set

• Primary Device ID: 10886333208958
• NIH Device Record Key: 5eb6ade9-f4a4-4265-91c1-2613825160fd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Identification Labels
• Version Model Number: 197823
• Catalog Number: 197823
• Company DUNS: 140727624
• Company Name: ARGON MEDICAL DEVICES, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00886333208951 [Primary]
GS1	10886333208958 [Package]; Contains: 00886333208951; Package: Box [5 Units]; In Commercial Distribution
GS1	20886333208955 [Package]; Package: Box [50 Units]; In Commercial Distribution

FDA Product Code

• LYN: Apparatus, Visual Reinforcement Audiometric

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-07-29
• Device Publish Date: 2022-07-21

Devices Manufactured by ARGON MEDICAL DEVICES, INC.

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• 20886333227512 - ClosureFast Introducer Sheath: 2024-08-06 ClosureFast Introducer Sheath Set 7Fr/Ch (2.3mm) x 7cm
• 20886333227529 - ClosureFast Introducer Sheath: 2024-08-06 ClosureFast™ Introducer Sheath Set 7Fr/Ch (2.3mm) x 11cm
• 20886333227550 - ClosureFast Micro Puncture: 2024-08-06 ClosureFast™ Micro Puncture Kit 4Fr/Ch (1.3mm)
• 20886333227567 - ClosureFast Micro Puncture: 2024-08-06 ClosureFast™ Micro Puncture Kit 5Fr/Ch (1.7mm)
• 20886333227574 - ClosureFast Tumescent Infiltration Kit: 2024-08-06 ClosureFast™ Tumescent Infiltration Kit