Home GUDID 00850083596002 LaserWrap
Primary DI 00850083596002
Brand LaserWrap
Company SPECTRA THERAPY, LLC
Model A-10
Catalog number A-10
Device description A-10 Slim Impulse Laser Unit with USB Cord and Charger for use with LASERwrap accessories. LASERwrap® is a wearable cold laser therapy device that consists of a small impulse laser unit that transmits light through filaments into a pad or wrap. The pad or wrap is applied to almost any part of the body, helping both human and animals. This type of therapy is also known as low level laser therapy, LLLT, or cold laser therapy.
Published 2026-07-24
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC true
Sterile false
Single use false
Product Codes# Code, Name table Code Name ILY Lamp, Infrared, Therapeutic Heating
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class ILY Lamp, Infrared, Therapeutic Heating Physical Medicine 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00850083596002 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00850083596002 00850083596002 850083596002 0850083596002
GMDN Terms# Term, Definition table Term Definition Musculoskeletal/physical therapy laser, professional An electrically-powered diode laser intended to provide non-surgical laser therapy [e.g., infrared phototherapy, low-level laser therapy (LLLT)] for localized treatment of musculoskeletal conditions (e.g., muscle/joint pain, sports injury), improvement of local blood circulation in the treated areas to facilitate healing, or for non-needle acupuncture. It typically consists of a control unit which may be mounted on a mobile trolley, a foot-switch, and a connected applicator/beam guide designed for intra-orifice (e.g., intravaginal) or transcutaneous delivery of visible red/infrared laser light energy/heat. It is intended to be operated exclusively by a healthcare professional.
Regulatory Flags# DUNS number 021300119 Device count 1 DM exempt false Premarket exempt true HCT/P false Kit false Combination product false Lot or batch false Serial number true Manufacturing date on label false Expiration date on label false Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use false Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00850083596026 LaserWrap A-100 A-100 2026-07-24
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