FDA UDI In Commercial Distribution 🇺🇸 United States

PALLAS Foot Switch

DI: 08800035500290 · Model: PALLAS Foot Switch · Laseroptek Co.,Ltd
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PALLAS Foot Switch
Primary DI
08800035500290
Version / Model
PALLAS Foot Switch
Company Name
Laseroptek Co.,Ltd
Labeler DUNS
689856875
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-01-15
Public Version
4
Public Version Date
2019-02-07
Public Version Status
Update
Public Device Record Key
88a64bdf-5d27-4a17-977d-39ae1c2a3f6a

Device Description

PALLAS Foot Switch

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
47882 Dermatological excimer laser system

Identifiers

Type ID
Primary 08800035500290

Premarket Submissions

Submission Number Supplement Number
K172639 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 40 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
20 – 80 Percent (%) Relative Humidity
Type
Handling Environment Temperature
Temperature Range
15 – 30 Degrees Celsius
Type
Handling Environment Humidity
Temperature Range
20 – 80 Percent (%) Relative Humidity