CHS 54-5030

GUDID 00628725002828

30CC Oral Syringe Non-sterile, enteral only syringe

Canadian Hospital Specialties Limited

ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use ENFit oral/enteral syringe, single-use

• Primary Device ID: 00628725002828
• NIH Device Record Key: df821650-24e1-4d75-80e5-86b1e56632e1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CHS
• Version Model Number: 54-5030
• Catalog Number: 54-5030
• Company DUNS: 240992693
• Company Name: Canadian Hospital Specialties Limited
• 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: true
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00628725002828 [Primary]
GS1	50628725002823 [Package]; Package: Corrugate Case [102 Units]; In Commercial Distribution

FDA Product Code

• KYX: Dispenser, Liquid Medication

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-07-24
• Device Publish Date: 2023-07-14

On-Brand Devices [CHS]

• 00628725002835: 50CC Oral Syringe Non-sterile, enteral only syringe
• 00628725002828: 30CC Oral Syringe Non-sterile, enteral only syringe
• 00628725002811: 20CC Oral Syringe Non-sterile, Enteral Only Syringe
• 00628725002804: 10CC Oral syringe non sterile, enteral only syringe
• 00628725002439: 5CC Oral syringe non sterile, enteral only syringe
• 00628725096322: RECTANGULAR WASH BASIN-TEAL (6 QUART/7 LITER)
• 50628725007392: INSUFFLATION TUBING, 22MM CONNECTOR
• 50628725007385: INSUFFLATION TUBING, LUER CONNECTOR
• 50628725007378: INSUFFLATION TUBING, QUICK CONNECTOR
• 50628725007361: INSUFFLATION TUBING,BARB CONNECTOR