FDA UDI In Commercial Distribution 🇺🇸 United States

SL3®

DI: D813ZLR10180 · Model: ZLR1018 · DEN-MAT HOLDINGS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
SL3®
Primary DI
D813ZLR10180
Version / Model
ZLR1018
Catalog Number
ZLR1018
Company Name
DEN-MAT HOLDINGS, LLC
Labeler DUNS
809857704
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-22
Public Version
1
Public Version Date
2022-09-30
Public Version Status
New
Public Device Record Key
b7f8f9fd-3bf7-4262-ab0f-306d36427250

Device Description

FIBERS AC-FIBER 400um 12FT

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
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
60340 Dental diode laser system

Identifiers

Type ID
Primary D813ZLR10180

Customer Contacts

Phone
18004336628