MICROSAFE

GUDID 00850059420331

MICROSAFE, 20 ul

DRUMMOND SCIENTIFIC COMPANY

Capillary blood collection tube IVD, lithium heparin

• Primary Device ID: 00850059420331
• NIH Device Record Key: 7d37d330-f7d5-4b21-86e2-af5cb9697696
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MICROSAFE
• Version Model Number: 1020
• Company DUNS: 002354272
• Company Name: DRUMMOND SCIENTIFIC COMPANY
• Device Count: 2000
• 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	00850059420096 [Primary]
GS1	00850059420331 [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 [MICROSAFE]

• 00850059420393: MICROSAFE, 10 ul
• 00850059420256: MICROSAFE, 80 ul
• 00850059420263: MICROSAFE, 75 ul
• 00850059420270: MICROSAFE, 60 ul
• 00850059420287: MICROSAFE, 50 ul
• 00850059420294: MICROSAFE, 40 ul
• 00850059420300: MICROSAFE, 35 ul
• 00850059420317: MICROSAFE, 30 ul
• 00850059420324: MICROSAFE, 25 ul
• 00850059420331: MICROSAFE, 20 ul
• 00850059420348: MICROSAFE, 17 ul
• 00850059420225: MICROSAFE, 15 ul
• 00850059420232: MICROSAFE, 10 ul short
• 00850059420249: MICROSAFE, 5 ul