eTwo System FG70503

GUDID 00817495024530

eTwo System

Candela Corporation

Multi-modality skin surface treatment system

• Primary Device ID: 00817495024530
• NIH Device Record Key: 69950a2b-9e3d-42ff-8d95-b067789680e6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: eTwo System
• Version Model Number: FG70503
• Catalog Number: FG70503
• Company DUNS: 053468385
• Company Name: Candela Corporation
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• Manufacturing Date: true
• 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: 8007352737
• Email: customerservice@syneron-candela.com
• Phone: 8007352737
• Email: customerservice@syneron-candela.com
• Phone: 8007352737
• Email: customerservice@syneron-candela.com
• Phone: 8007352737
• Email: customerservice@syneron-candela.com
• Phone: 8007352737
• Email: customerservice@syneron-candela.com
• Phone: 8007352737
• Email: customerservice@syneron-candela.com
• Phone: 8007352737
• Email: customerservice@syneron-candela.com
• Phone: 8007352737
• Email: customerservice@syneron-candela.com
• Phone: 8007352737
• Email: customerservice@syneron-candela.com
• Phone: 8007352737
• Email: customerservice@syneron-candela.com
• Phone: 8007352737
• Email: customerservice@syneron-candela.com
• Phone: 8007352737
• Email: customerservice@syneron-candela.com
• Phone: 8007352737
• Email: customerservice@syneron-candela.com
• Phone: 8007352737
• Email: customerservice@syneron-candela.com
• Phone: 8007352737
• Email: customerservice@syneron-candela.com
• Phone: 8007352737
• Email: customerservice@syneron-candela.com
• Phone: 8007352737
• Email: customerservice@syneron-candela.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817495024530 [Primary]
GS1	07290109952864 [Previous]

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

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: 2023-10-30
• Device Publish Date: 2023-10-20

Devices Manufactured by Candela Corporation

• 00817495023977 - ASSY, ACC HAND PIECE, LARGE SPOT, GMPP: 2024-09-05 ASSY, ACC HAND PIECE, LARGE SPOT, GMPP
• 00817495024028 - ASSY, DCD HAND PIECE, LARGE SPOT, GMPP: 2024-09-05 ASSY, DCD HAND PIECE, LARGE SPOT, GMPP
• 00817495024035 - GMPP DCD Large Spot Option Kit, w/HP, w/SAs, w/Fiber Assembly: 2024-09-05 GMPP DCD Large Spot
• 00817495024042 - GMPP ACC Large Spot Option Kit, w/HP, w/SAs, w/Fiber Assembly: 2024-09-05 GMPP ACC Large Spot
• 00817495024011 - MSDS DCD Option Kit GMPP: 2024-07-04 MSDS DCD Option Kit GMPP
• 00817495023946 - Modified LSDS Fiber Assembly, 12-26 mm: 2024-06-25 Modified LSDS Fiber Assembly 12-26 mm
• 00817495023984 - GentleCool Pro Canister Cryogen (R134a / 980g / US): 2024-05-31 Canister Cryogen (R134a / 980g / US)
• 00817495024004 - GentleCool Pro Packaged 15-Pack of Cryogen (R134a / 980g / US): 2024-05-31 Packaged 15-Pack of Cryogen (R134a / 980g / US)