Panosol 6-3D

GUDID 00850054882134

UVB-612

DAAVLIN DISTRIBUTING CO., THE

Ultraviolet phototherapy unit, professional
Primary Device ID00850054882134
NIH Device Record Key020afda2-f2ff-4728-97a3-0f19263a432f
Commercial Distribution StatusIn Commercial Distribution
Brand NamePanosol 6-3D
Version Model NumberPanosol 6-3D
Company DUNS056696347
Company NameDAAVLIN DISTRIBUTING CO., THE
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)322-8546
Emailinfo@daavlin.com
Phone+1(800)322-8546
Emailinfo@daavlin.com
Phone+1(800)322-8546
Emailinfo@daavlin.com
Phone+1(800)322-8546
Emailinfo@daavlin.com
Phone+1(800)322-8546
Emailinfo@daavlin.com
Phone+1(800)322-8546
Emailinfo@daavlin.com
Phone+1(800)322-8546
Emailinfo@daavlin.com
Phone+1(800)322-8546
Emailinfo@daavlin.com
Phone+1(800)322-8546
Emailinfo@daavlin.com
Phone+1(800)322-8546
Emailinfo@daavlin.com
Phone+1(800)322-8546
Emailinfo@daavlin.com
Phone+1(800)322-8546
Emailinfo@daavlin.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100850054882134 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FTCLIGHT, ULTRAVIOLET, DERMATOLOGICAL

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-12-20
Device Publish Date2024-12-12

On-Brand Devices [Panosol 6-3D]

00850054882141UVB-680
00850054882134UVB-612
00850054882127UVA-680
00850054882110UVA-612

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