Candela GentleMax Pro Plus - DRAP MDIR-0008516 (Class C)

DRAP REGISTERED MEDICAL DEVICE

Candela GentleMax Pro Plus (Laser Machine) is registered with DRAP under number MDIR-0008516 as a Class C (moderate to high risk) medical device, imported. The listed holder is Aesthetic Life. It is listed as valid until 25 Mar 2030.

Screening result

i
Imported device, registered with DRAP as Class C (moderate to high risk)
MDIR-0008516 · the class is taken from DRAP's list for this number
✓
Found in DRAP's published list
DRAP registered Class B/C/D list, 28 Aug 2025
✓
Listed valid until 25 Mar 2030
i
Holder not found in DRAP's published licence list
That list covers manually issued licences only. Ask for a copy of the establishment licence.
DeviceCandela GentleMax Pro Plus (Laser Machine)
ClassC
Listed holderAesthetic Life
Holder address4th Floor, Plot 16-C, Ittehad Commercial Area, Khayaban-e- Nishat, DHA Phase-VI, Karachi
Manufacturing siteM/s Candela Corporation 251 Locke Drive, Marlborough, MA 01752, USA M/s Jabil Circuit (Shanghai) Ltd 500 Tian Lin Road Shanghai, China 200233
Issued26 Mar 2025
Renewal date25 Mar 2030

Specifications

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Screened 6 Oct 2026, 18:01 (Pakistan time). A screening aid, not an official DRAP verification.

More devices from this holder

Other DRAP registrations and enlistments listed for the same company.

MDIR-0007671Profhilo Hilow Hyaluronic Acid Sodium Salt for Intradermal Use [Profhilo 3,2% - 32MG (II-HA) + 32…Class D
MDIR-0007672Profhilo Body Hilow Hyaluronic Acid Sodium Salt for Intradermal Use [Profhilo 3,2% - 48MG (II-HA) +…Class D
MDIR-0007854Ultra-Z Ultrasonic Surgical UniClass C
MDIR-0008517Candela GentleYag Pro-U (Laser Machine) [9914-00-9020]Class C

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Source: DRAP's published provisional lists. A screening aid, not an official DRAP verification; confirm with DRAP and the supplier's original documents.