Parallel Compressor F004.0009

GUDID B922F00400090

Parallel Compressor

INDIUS MEDICAL TECHNOLOGIES PRIVATE LIMITED

Internal spinal fixation procedure kit, reusable

• Primary Device ID: B922F00400090
• NIH Device Record Key: 697fdf6d-22b2-4338-b4ec-9202f5ba547f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Parallel Compressor
• Version Model Number: F004.0009
• Catalog Number: F004.0009
• Company DUNS: 860396609
• Company Name: INDIUS MEDICAL TECHNOLOGIES PRIVATE 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: false
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1636-825-1231
• Email: info@indiusmedical.com
• Phone: +1636-825-1231
• Email: info@indiusmedical.com
• Phone: +1636-825-1231
• Email: info@indiusmedical.com
• Phone: +1636-825-1231
• Email: info@indiusmedical.com
• Phone: +1636-825-1231
• Email: info@indiusmedical.com
• Phone: +1636-825-1231
• Email: info@indiusmedical.com
• Phone: +1636-825-1231
• Email: info@indiusmedical.com
• Phone: +1636-825-1231
• Email: info@indiusmedical.com
• Phone: +1636-825-1231
• Email: info@indiusmedical.com
• Phone: +1636-825-1231
• Email: info@indiusmedical.com
• Phone: +1636-825-1231
• Email: info@indiusmedical.com
• Phone: +1636-825-1231
• Email: info@indiusmedical.com
• Phone: +1636-825-1231
• Email: info@indiusmedical.com
• Phone: +1636-825-1231
• Email: info@indiusmedical.com
• Phone: +1636-825-1231
• Email: info@indiusmedical.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B922F00400090 [Primary]

FDA Product Code

• HWN: Instrument, Compression

Sterilization

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

[B922F00400090]

Moist Heat or Steam Sterilization

[B922F00400090]

Moist Heat or Steam Sterilization

[B922F00400090]

Moist Heat or Steam Sterilization

[B922F00400090]

Moist Heat or Steam Sterilization

[B922F00400090]

Moist Heat or Steam Sterilization

[B922F00400090]

Moist Heat or Steam Sterilization

[B922F00400090]

Moist Heat or Steam Sterilization

[B922F00400090]

Moist Heat or Steam Sterilization

[B922F00400090]

Moist Heat or Steam Sterilization

[B922F00400090]

Moist Heat or Steam Sterilization

[B922F00400090]

Moist Heat or Steam Sterilization

[B922F00400090]

Moist Heat or Steam Sterilization

[B922F00400090]

Moist Heat or Steam Sterilization

[B922F00400090]

Moist Heat or Steam Sterilization

[B922F00400090]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-03-11
• Device Publish Date: 2022-03-03

On-Brand Devices [Parallel Compressor]

• B922F00400090: Parallel Compressor
• B922F004004709: Parallel Compressor