PW19F

GUDID 00849771037057

INSTRUMENT TRAY WITH ROLLED BEAD 48 X 32 X 2CM [1/EA]

KEY SURGICAL, INC.

Instrument tray, reusable

• Primary Device ID: 00849771037057
• NIH Device Record Key: 7eb1c62e-4e1f-46ca-9814-adc02ac7c6ee
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: PW19F
• Catalog Number: PW19F
• Company DUNS: 604056226
• Company Name: KEY SURGICAL, 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: false
• Lot Batch: true
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)541-7995
• Email: regulatory@keysurgical.com
• Phone: +1(800)541-7995
• Email: regulatory@keysurgical.com
• Phone: +1(800)541-7995
• Email: regulatory@keysurgical.com
• Phone: +1(800)541-7995
• Email: regulatory@keysurgical.com
• Phone: +1(800)541-7995
• Email: regulatory@keysurgical.com
• Phone: +1(800)541-7995
• Email: regulatory@keysurgical.com
• Phone: +1(800)541-7995
• Email: regulatory@keysurgical.com
• Phone: +1(800)541-7995
• Email: regulatory@keysurgical.com
• Phone: +1(800)541-7995
• Email: regulatory@keysurgical.com
• Phone: +1(800)541-7995
• Email: regulatory@keysurgical.com
• Phone: +1(800)541-7995
• Email: regulatory@keysurgical.com
• Phone: +1(800)541-7995
• Email: regulatory@keysurgical.com
• Phone: +1(800)541-7995
• Email: regulatory@keysurgical.com
• Phone: +1(800)541-7995
• Email: regulatory@keysurgical.com
• Phone: +1(800)541-7995
• Email: regulatory@keysurgical.com
• Phone: +1(800)541-7995
• Email: regulatory@keysurgical.com
• Phone: +1(800)541-7995
• Email: regulatory@keysurgical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00849771037057 [Primary]

FDA Product Code

• FSM: TRAY, SURGICAL, INSTRUMENT

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: 2023-11-10
• Device Publish Date: 2023-11-02

Devices Manufactured by KEY SURGICAL, INC.

• 00849771052708 - NA: 2026-01-27 Plastic Sterilization Tray with Slotted Base and Silicone Mat; 7.5-inch x 2.5-inch x 0.75-inch 190.5 x 63.5 x 19mm
• 00849771052159 - NA: 2025-08-27 Dry Endoscopy Sponge, 2-inch OD x 0.50-inch ID x 3.75-inch Long
• 00849771048237 - NA: 2025-08-19 K-Wire and Steinmann Pin Dispensers, 5/64-inch (2.0mm) diameter, Holds pins up to 12-inch long
• 00849771049036 - NA: 2025-08-19 K-Wires, Single trocar, .035-inch (.9mm) diameter, 4-inch long
• 00849771049289 - NA: 2025-08-19 K-Wires, Single trocar, .062-inch (1.6mm) diameter, 6-inch long
• 00849771049500 - NA: 2025-08-19 K-Wires, Single diamond, round end, .062-inch (1.6mm) diameter, 12-inch
• 00849771048169 - NA: 2025-05-08 K-Wire and Steinmann Pin Dispensers, .035 inch .9mm diameter, Holds kwires up to 6 inch long
• 00849771049012 - NA: 2025-05-08 K-Wires, Double trocar, .054-inch (1.4mm) diameter, 12-inch long