Tubing, with filter, sterile, for insuflation ONG04199ST119

GUDID 03700512905080

Promepla

Surgical irrigation/aspiration tubing set

• Primary Device ID: 03700512905080
• NIH Device Record Key: f98403ba-1eba-495b-901f-0a41df03c1e2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Tubing, with filter, sterile, for insuflation
• Version Model Number: WA95005A
• Catalog Number: ONG04199ST119
• Company DUNS: 401020409
• Company Name: Promepla
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	03700512905080 [Primary]
GS1	14042761072639 [Package]; Package: Box [20 Units]; In Commercial Distribution

FDA Product Code

• NKC: Tubing/Tubing With Filter, Insufflation, Laparoscopic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2020-07-07
• Device Publish Date: 2016-09-23

On-Brand Devices [Tubing, with filter, sterile, for insuflation]

• 04042761072632: WA95005A
• 03700512905080: WA95005A