AccessGUDID - DEVICE: TRUMPF MEDICAL (00887761980112)

GUDID

Device Identifier (DI) Information

Brand Name: TRUMPF MEDICAL
Version or Model: 4028150
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: Baxter Medical Systems GmbH + Co. KG

Primary DI Number: 00887761980112
Issuing Agency: GS1
Commercial Distribution End Date: May 06, 2024
Device Count: 1
Labeler D-U-N-S® Number*: 330961223 *Terms of Use

Device Description: VidiaPort Springarm Bottom

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
32245	Medical monitor/light mount	A permanently-fixed structure designed to support a light and/or an image display monitor that is used for medical purposes [e.g., in an operating room (OR) and/or an examination/treatment room]. The mount is intended to be permanently-fixed to the ceiling and/or wall. This device will be designed to enable dynamic positioning (e.g., with dynamic arms, sliding bracket); the device to be mounted (medical light/monitor) is not included.	Active	false
32288	Surgical camera holder	A device designed to hold or stabilize a video camera or endoscope while recording a surgical operative procedure. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FQP	Lamp, operating-room
FTD	Lamp, surgical
FSY	Light, surgical, ceiling mounted
FSQ	Light, surgical, instrument

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 51e3a39c-adef-4094-af14-6dcb27fd73ea
Public Version Date: November 05, 2024
Public Version Number: 3
DI Record Publish Date: November 29, 2022