TL 5000/3000 – Surgical Light

GUDID 00887761968448

TruLight 5000 / 3000 Ceiling Single

TRUMPF Medizin Systeme GmbH + Co. KG

Operating room light Operating room light Operating room light Operating room light Operating room light Operating room light
Primary Device ID00887761968448
NIH Device Record Key12056c93-ad79-413d-bf9a-112ba29b7261
Commercial Distribution StatusIn Commercial Distribution
Brand NameTL 5000/3000 – Surgical Light
Version Model Number4038110
Company DUNS330961223
Company NameTRUMPF Medizin Systeme GmbH + Co. KG
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+4936715860
EmailSURGICAL@HILLROM.COM
Phone+4936715860
EmailSURGICAL@HILLROM.COM
Phone+4936715860
EmailSURGICAL@HILLROM.COM
Phone+4936715860
EmailSURGICAL@HILLROM.COM
Phone+4936715860
EmailSURGICAL@HILLROM.COM
Phone+4936715860
EmailSURGICAL@HILLROM.COM

Device Identifiers

Device Issuing AgencyDevice ID
GS100887761968448 [Primary]

FDA Product Code

FSYLight, surgical, ceiling mounted

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-01-13
Device Publish Date2023-01-05

On-Brand Devices [TL 5000/3000 – Surgical Light]

00887761968448TruLight 5000 / 3000 Ceiling Single
00887761968431TruLight 5000 / 3000 Mobile
00887761968424TruLight 5000 / 3000 Wall
00887761968417TruLight 5000 / 3000 Pendant
00887761968400TruLight 5000 / 3000 Ceiling Duo
00887761968394TruLight 5000 / 3000 Ceiling Trio
00887761968387TruLight 5000 / 3000 Ceiling Quad

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.