MEDTRONIC

GUDID 01618125160739

Medtronic Navigation Inc. Equipment Covers Clear Polyethylene Sterile 16in x 48in x 1in 25 per Case

TIDI PRODUCTS, LLC

Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use Patient surgical drape, single-use

• Primary Device ID: 01618125160739
• NIH Device Record Key: 3490ff2a-490e-41d4-aae2-841baaef45e4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MEDTRONIC
• Version Model Number: 25847
• Company DUNS: 063519193
• Company Name: TIDI PRODUCTS, LLC
• 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: 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	00618125160730 [Package]; Package: [25 Units]; In Commercial Distribution
GS1	01618125160739 [Primary]

FDA Product Code

• KKX: Drape, Surgical

Sterilization

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

[01618125160739]

Ethylene Oxide

[01618125160739]

Ethylene Oxide

[01618125160739]

Ethylene Oxide

[01618125160739]

Ethylene Oxide

[01618125160739]

Ethylene Oxide

[01618125160739]

Ethylene Oxide

[01618125160739]

Ethylene Oxide

[01618125160739]

Ethylene Oxide

[01618125160739]

Ethylene Oxide

[01618125160739]

Ethylene Oxide

[01618125160739]

Ethylene Oxide

[01618125160739]

Ethylene Oxide

[01618125160739]

Ethylene Oxide

[01618125160739]

Ethylene Oxide

[01618125160739]

Ethylene Oxide

[01618125160739]

Ethylene Oxide

[01618125160739]

Ethylene Oxide

[01618125160739]

Ethylene Oxide

[01618125160739]

Ethylene Oxide

[01618125160739]

Ethylene Oxide

[01618125160739]

Ethylene Oxide

[01618125160739]

Ethylene Oxide

[01618125160739]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2021-02-05
• Device Publish Date: 2016-10-07

On-Brand Devices [MEDTRONIC]

• 01618125160739: Medtronic Navigation Inc. Equipment Covers Clear Polyethylene Sterile 16in x 48in x 1in 25 per C
• 01618125152031: Medtronic Navigation Inc. Equipment Covers Clear Polyethylene Sterile 10in x 102in x 1in 25 per
• 00618125160730: Medtronic Navigation Inc. Equipment Covers Clear Polyethylene Sterile 16in x 48in x 1in 25 per C
• 10618125152367: Medtronic Navigation Inc. Mouse Covers Clear Polyethylene Sterile 1in x 1in x 1in 15 per Case
• 00618125152032: Drape, AxIEM Emitter