MICROSUTURE

GUDID 00812444029031

Suture

RIVERPOINT MEDICAL, LLC

Nylon suture, non-bioabsorbable, monofilament

• Primary Device ID: 00812444029031
• NIH Device Record Key: 3c26a5bc-f817-4744-84a2-b43c86bc704a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MICROSUTURE
• Version Model Number: GEM395BKC
• Company DUNS: 964053560
• Company Name: RIVERPOINT MEDICAL, LLC
• Device Count: 1
• 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: 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	00812444029031 [Primary]
GS1	10812444029038 [Package]; Package: [12 Units]; In Commercial Distribution

FDA Product Code

• GAR: Suture, Nonabsorbable, Synthetic, Polyamide

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-02-18
• Device Publish Date: 2019-01-17

On-Brand Devices [MICROSUTURE]

• 00812444029031: Suture
• 10812444029021: Suture
• 10812444029014: Suture
• 00812444029000: Suture
• 10812444026235: Suture
• 10812444024538: SUTURE
• 10812444024521: Suture
• 10812444024484: SUTURE
• 10812444024477: SUTURE
• 10812444024460: SUTURE
• 00812444022896: SUTURE
• 00812444022889: SUTURE
• 10812444022879: SUTURE
• 10812444022862: SUTURE
• 10812444022855: SUTURE
• 10812444022848: SUTURE
• 10812444022831: SUTURE
• 10812444020103: SUTURE
• 00810020084108: Suture
• 10810020084099: Suture