TPAK TM-310

GUDID 00855204008051

Tension Pneumothorax Decompression Needle: 10 gauge x 3.25"

TYTEK MEDICAL INC.

Body aspiration needle, single-use

• Primary Device ID: 00855204008051
• NIH Device Record Key: da7a224b-5110-49e5-9539-834607059213
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TPAK
• Version Model Number: TM-310
• Catalog Number: TM-310
• Company DUNS: 078589992
• Company Name: TYTEK MEDICAL INC.
• 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: true
• 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	00855204008051 [Primary]

FDA Product Code

• GAA: Needle, Aspiration And Injection, Disposable

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: 2019-10-11
• Device Publish Date: 2019-10-03

On-Brand Devices [TPAK]

• 00855204008051: Tension Pneumothorax Decompression Needle: 10 gauge x 3.25"
• 00855204008006: Tension Pneumothorax Decompression Needle: 14 gauge x 3.25"