HYPERION body

Primary DI
08800035500504
Brand
HYPERION body
Company
Laseroptek Co.,Ltd
Model
HYPERION body
Device description
HYPERION body
Published
2018-01-12
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Product Codes#

Code, Name table
CodeName
GEXPowered Laser Surgical Instrument

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GEXPowered Laser Surgical InstrumentGeneral, Plastic Surgery2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K132286000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K132286000HYPERION LONG PULSED ND: YAG LASERScarlet Rf, Inc.2014-01-22GEX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
08800035500504PackageGS11In Commercial Distribution
08800035500412PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
08800035500504088000355005048800035500504
08800035500412088000355004128800035500412

GMDN Terms#

Term, Definition table
TermDefinition
Dermatological solid-state laser systemA mains electricity (AC-powered) device assembly in which input energy (e.g., flashlamp, diode laser) is used to excite a glass/crystal rod, or a fibre doped with a glass/crystal element (known as fibre laser), to emit a high-power laser beam intended to incise, excise, ablate, and vaporize soft tissues for dermatological applications such as skin resurfacing, acne treatment, and/or lesion/hair/tattoo removal; some types may also be used for coagulation/haemostasis procedures. It typically includes a light source, laser beam delivery/positioning device(s), user interface, and controls/foot-switch; it does not include frequency-doubling technology.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Handling Environment Humidity20 Percent (%) Relative Humidity80 Percent (%) Relative Humidity

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
689856875
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
false
Serial number
true
Manufacturing date on label
true
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 DIBrandModelCatalogPublished
08800035500412HYPERION bodyHYPERION body2018-01-12
08800035500306HYPERION power cableHYPERION power cable2018-01-12
08800035500429HYPERION ArmHYPERION Arm2018-01-12
08800035500436HYPERION Gold HandpieceHYPERION Gold Handpiece2018-01-12
08800035500443HYPERION Red HandpieceHYPERION Red Handpiece2018-01-12
08800035500450HYPERION Blue HandpieceHYPERION Blue Handpiece2018-01-12
08800035500467HYPERION User ManualHYPERION User Manual2018-01-12
08800035500474HYPERION Service ManualHYPERION Service Manual2018-01-12
08800035500481HYPERION Foot SwitchHYPERION Foot Switch2018-01-12
08800035500511HYPERION FIBERHYPERION FIBER2018-04-16
08800035500788HELIOS III bodyHELIOS III body2019-11-21
08800035501860HELIOS 785 Pico BodyHELIOS 785 Pico (1754V2) Body2025-02-18
08800035500740HELIOS III bodyHELIOS III body2019-11-21
08800035500795HELIOS III ArmHELIOS III Arm2019-11-21
08800035500801HELIOS III Zoom HandpieceHELIOS III Zoom Handpiece2019-11-21
08800035500818HELIOS III 532 HandpieceHELIOS III 532 Handpiece2019-11-21
08800035500825HELIOS III 1064 HandpieceHELIOS III 1064 Handpiece2019-11-21
08800035500832HELIOS III Collimator HandpieceHELIOS III Collimator Handpiece2019-11-21
08800035500849HELIOS III User ManualHELIOS III User Manual2019-11-21
08800035500856HELIOS III Service ManualHELIOS III Service Manual2019-11-21

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