SAFECAP

GUDID 00850059420379

SAFECAP, Precalibrated

DRUMMOND SCIENTIFIC COMPANY

Capillary blood collection tube IVD, lithium heparin

• Primary Device ID: 00850059420379
• NIH Device Record Key: 4ee1a407-cc83-42b9-ba7b-aab0186b9c2e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SAFECAP
• Version Model Number: R60-2000M
• Company DUNS: 002354272
• Company Name: DRUMMOND SCIENTIFIC COMPANY
• Device Count: 20
• 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: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850059420027 [Primary]
GS1	00850059420379 [Unit of Use]

FDA Product Code

• GIO: TUBE, COLLECTION, CAPILLARY BLOOD

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: 2024-05-27
• Device Publish Date: 2024-05-17

On-Brand Devices [SAFECAP]

• 00850059420379: SAFECAP, Precalibrated
• 00850059420362: SAFECAP, Plain
• 00850059420355: SAFECAP, Heparanized