FDA UDI In Commercial Distribution 🇺🇸 United States

CuRAS Collimation H/P

DI: 08800023200683 · Model: QND Collimation H/P · ILOODA.CO.,LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CuRAS Collimation H/P
Primary DI
08800023200683
Version / Model
QND Collimation H/P
Company Name
ILOODA.CO.,LTD
Labeler DUNS
631129749
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-24
Public Version
2
Public Version Date
2021-08-24
Public Version Status
Update
Public Device Record Key
f8cba289-8876-4d06-ac00-7694fd8a406b

Device Description

QND Collimation H/P

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 08800023200683

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K173038 000