Geri-Gentle

GUDID 20369771000218

IV ADMINISTRATION SET

GERI-GENTLE CORPORATION

Intravenous fluid bag spike Intravenous fluid bag spike

• Primary Device ID: 20369771000218
• NIH Device Record Key: c04994f5-14e6-492f-a691-f0a70c6919ea
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Geri-Gentle
• Version Model Number: 1221
• Company DUNS: 361663839
• Company Name: GERI-GENTLE CORPORATION
• Device Count: 300
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10369771000214 [Unit of Use]
GS1	20369771000218 [Primary]

FDA Product Code

• FPA: Set, Administration, Intravascular

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-02-02

Devices Manufactured by GERI-GENTLE CORPORATION

• 00369771003659 - Sharps Collector 5QT: 2023-11-09 Sharps Collector 5QT
• 00369771003390 - Pen Needle: 2023-09-11 Safety Pen Needle 30G
• 00369771003437 - Prefilled Syrings: 2023-09-11 10ML PREFILLED SYRINGE
• 00369771003161 - Oxygen Concentrator: 2023-08-09 Oxygen Concentrator
• 20369771000782 - Lancets Safety: 2023-08-09 Lancets Safety
• 00369771003123 - SYRINGE RETRACT U100 1cc 29x.5: 2023-07-10 SYRINGE RETRACT U100 1cc 29x.5
• 20369771000898 - Syringes Safety: 2023-02-22 SYR U100 1cc 29x.5
• 20369771000904 - Syringes Safety: 2023-02-22 SYR U100 .5cc 29x.5