ASSY, CABLE, THERAPY, LP35 11113-000007

GUDID 00883873783566

ASSY, CABLE, THERAPY, LP35

PHYSIO-CONTROL, INC.

External defibrillation electrode, adult, reusable

• Primary Device ID: 00883873783566
• NIH Device Record Key: 77bbb253-4e3e-4a27-b013-1f6ac3159bbd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ASSY, CABLE, THERAPY, LP35
• Version Model Number: 11113
• Catalog Number: 11113-000007
• Company DUNS: 009251992
• Company Name: PHYSIO-CONTROL, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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)442-1142
• Email: rs.seacustomersupport@stryker.com
• Phone: +1(800)442-1142
• Email: rs.seacustomersupport@stryker.com
• Phone: +1(800)442-1142
• Email: rs.seacustomersupport@stryker.com
• Phone: +1(800)442-1142
• Email: rs.seacustomersupport@stryker.com
• Phone: +1(800)442-1142
• Email: rs.seacustomersupport@stryker.com
• Phone: +1(800)442-1142
• Email: rs.seacustomersupport@stryker.com
• Phone: +1(800)442-1142
• Email: rs.seacustomersupport@stryker.com
• Phone: +1(800)442-1142
• Email: rs.seacustomersupport@stryker.com
• Phone: +1(800)442-1142
• Email: rs.seacustomersupport@stryker.com
• Phone: +1(800)442-1142
• Email: rs.seacustomersupport@stryker.com
• Phone: +1(800)442-1142
• Email: rs.seacustomersupport@stryker.com
• Phone: +1(800)442-1142
• Email: rs.seacustomersupport@stryker.com
• Phone: +1(800)442-1142
• Email: rs.seacustomersupport@stryker.com
• Phone: +1(800)442-1142
• Email: rs.seacustomersupport@stryker.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00883873783566 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P160026

FDA Product Code

• MKJ: Automated external defibrillators (non-wearable)

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: 2024-06-28
• Device Publish Date: 2024-06-20

Devices Manufactured by PHYSIO-CONTROL, INC.

• 00883873760031 - BATTERY, LI-ION, LP35: 2025-10-06
• 00883873760048 - SHIP KIT, POWER SUPPLY, LP35: 2025-10-06
• 00883873760420 - ASSY,CABLE,ADAPTER,TEMPERATURE,M-PAK,LP35,10FT: 2025-10-06
• 00883873760437 - ASSY, CABLE, ADAPTER, TEMP, LP35, 6FT,IRONGAN: 2025-10-06
• 00883873760444 - ASSY, CABLE, ADAPTER, IP, ICU, LP35: 2025-10-06
• 00883873760451 - ASSY, CABLE, ADAPTER, IP, EDWARDS, LP35: 2025-10-06
• 00883873760475 - CHARGER, BATTERY, LP35: 2025-10-06
• 00883873760482 - BATTERY, LI-ION, WITH IFU, LP35: 2025-10-06