FDA UDI In Commercial Distribution 🇺🇸 United States

Picocare

DI: 08800022303200 · Model: Picocare · WONTECH CO.,LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Picocare
Primary DI
08800022303200
Version / Model
Picocare
Company Name
WONTECH CO.,LTD
Labeler DUNS
695658263
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-08-11
Public Version
5
Public Version Date
2023-03-01
Public Version Status
Update
Public Device Record Key
f7cc0d9c-279a-4df6-b1fd-bf1dcecb2839

Device Description

Q-switched Nd:YAG Laser

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEX Powered Laser Surgical Instrument

GMDN Terms

Code Name
47877 Dermatological frequency-doubled solid-state laser system

Identifiers

Type ID
Primary 08800022303200

Premarket Submissions

Submission Number Supplement Number
K162755 000