FDA UDI In Commercial Distribution 🇺🇸 United States

Q-MASTER

DI: 08800042100001 · Model: Q-MASTER · AMI Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Q-MASTER
Primary DI
08800042100001
Version / Model
Q-MASTER
Company Name
AMI Inc.
Labeler DUNS
689004697
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-06-15
Public Version
2
Public Version Date
2021-08-24
Public Version Status
Update
Public Device Record Key
57e2d127-a15d-42e7-900f-5cbe52d0a1a8

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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 08800042100001

Customer Contacts

Phone
+82232819091

Premarket Submissions

Submission Number Supplement Number
K172908 000