Endoscopy Kit - Compliance

GUDID 00850025860284

Endoscopy Kit - Compliance

Micro-tech Usa

Endoscopy preparation kit

• Primary Device ID: 00850025860284
• NIH Device Record Key: c1ef26b4-3aa7-42d9-8ddf-3bd63ea978b9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Endoscopy Kit - Compliance
• Version Model Number: KT1A0004A
• Company DUNS: 079873914
• Company Name: Micro-tech Usa
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850025860277 [Primary]
GS1	00850025860284 [Package]; Contains: 00850025860277; Package: Box [30 Units]; In Commercial Distribution
GS1	00850025860291 [Package]; Package: Case [4 Units]; In Commercial Distribution

FDA Product Code

• KMJ: Lubricant, Patient

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: 2025-03-11
• Device Publish Date: 2025-03-03

On-Brand Devices [Endoscopy Kit - Compliance]

• 00858276007533: Endoscopy Kit - Compliance
• 00850025860284: Endoscopy Kit - Compliance