AccessGUDID - DEVICE: Pre-Install Set (00887761968127)

GUDID

Device Identifier (DI) Information

Brand Name: Pre-Install Set
Version or Model: 4068051
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: Baxter Medical Systems GmbH + Co. KG

Primary DI Number: 00887761968127
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 330961223 *Terms of Use

Device Description: Pre-Install Set iLED 7

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?
35954	Medical device rail	A device in the form of a narrow bar designed to be fixed on the wall for mounting and organizing medical devices [e.g., in hospital wards, treatment rooms, intensive care units (ICU)]; the equipment to be supported is not included. It may be used in conjunction with clamps and/or poles. It is available in various lengths.	Active	false

FDA Product Code

[?]

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

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: 6ff9756b-13e1-4a49-a430-3f25b8d04a82
Public Version Date: December 11, 2024
Public Version Number: 3
DI Record Publish Date: December 15, 2022