Nemoto

GUDID 14719879057192

Pacific Hospital Supply Company Limited

Angiography kit

• Primary Device ID: 14719879057192
• NIH Device Record Key: fed23da3-77de-4adc-b09f-08d01d2c070d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nemoto
• Version Model Number: TM0539K
• Company DUNS: 656117801
• Company Name: Pacific Hospital Supply Company Limited
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04719879057195 [Primary]
GS1	14719879057192 [Package]; Contains: 04719879057195; Package: [25 Units]; In Commercial Distribution
GS1	24719879057199 [Package]; Package: [50 Units]; In Commercial Distribution

FDA Product Code

• DXT: Injector And Syringe, Angiographic

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: 2024-09-18
• Device Publish Date: 2024-09-10

On-Brand Devices [Nemoto]

• 14719879052012: TM0539L
• 14719879057192: TM0539K
• 14719879053712: TM0539AQ
• 14719879052173: TM0544C
• 14719879052067: TM0539S
• 14719879052029: TM0539M
• 14719873437075: TM0539AE
• 14719873433534: TM0539003
• 14719873431967: TM0539P
• 24719879052354: TM0544W
• 14719873437099: TM0539010