AccessGUDID - DEVICE: InMode RF hand piece (07290019863298)

GUDID

Device Identifier (DI) Information

Brand Name: InMode RF hand piece
Version or Model: HP172296A
Commercial Distribution Status: In Commercial Distribution
Catalog Number: HP172296A
Company Name: INMODE M.D LTD

Primary DI Number: 07290019863298
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 600417351 *Terms of Use

Device Description: InModeRF HP 17x22x46 black

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
48005	Radio-frequency fat liquefaction system	An assembly of devices using radio-frequency (RF) energy for simultaneous adipose tissue liquefaction, blood vessel coagulation, and skin tightening during a radio-frequency-assisted liposuction (RFAL) procedure [lipectomy], typically performed for body contouring. The system consists of an RF-generating control unit that supplies RF energy to a dedicated applicator (handpiece) and provides continuous tissue temperature monitoring; impedance and power monitoring with tissue overheating safety systems; the RF applicator; and a foot-switch to control the RF energy supply. The liquified tissue is aspirated with an independent external suction system.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GEI	Electrosurgical, Cutting & Coagulation & Accessories

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K240780	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Handling Environment Humidity: between 10 and 90 Percent (%) Relative Humidity
Handling Environment Temperature: between 10 and 35 Degrees Celsius
Storage Environment Humidity: between 10 and 90 Percent (%) Relative Humidity
Storage Environment Temperature: between 10 and 35 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: f3b32b5a-fcf2-46c1-8c73-2a1502f63043
Public Version Date: February 28, 2025
Public Version Number: 1
DI Record Publish Date: February 20, 2025

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
No Package DIs found

Secondary DI

[?]

Issuing Agency [?]	Secondary DI Number
No Secondary DIs found

Unit of Use DI

[?]

Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]

Device Subject to Direct Marking (DM), but Excepted: Yes
DM DI Different from Primary DI: No
DM DI Number: None
CLOSE

Production Identifier(s) in UDI

[?]

Lot or Batch Number: Yes
Serial Number: No
Expiration Date: Yes
Manufacturing Date: Yes
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: 1-887-367-4556
Email: contact@inmode.com

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