AccessGUDID - DEVICE: TS 7500 (00887761974067)

GUDID

Device Identifier (DI) Information

Brand Name: TS 7500
Version or Model: 1854087
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: Baxter Medical Systems GmbH + Co. KG

Primary DI Number: 00887761974067
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 330961223 *Terms of Use

Device Description: TruSystem 7500 Hybrid Plus (FC)

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?
42558	Electromechanical operating table base	An electrically-powered component of a modular electromechanical operating table assembly designed as a height-adjustable support intended for the introduction and engagement of interchangeable operating table tops. It may be mobile or stationary and in the form of a column or frame.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
JEA	TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, AC-POWERED
KXJ	Table, radiologic
GDC	TABLE, OPERATING-ROOM, ELECTRICAL

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: 2ae0f41d-a6eb-4150-9f48-0068eea00b0c
Public Version Date: February 09, 2023
Public Version Number: 2
DI Record Publish Date: January 05, 2023

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
No Package DIs found

Secondary DI

[?]

Issuing Agency [?]	Secondary DI Number
No Secondary DIs found

Unit of Use DI

[?]

Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]

Device Subject to Direct Marking (DM), but Excepted: No
DM DI Different from Primary DI: No
DM DI Number: None
CLOSE

Production Identifier(s) in UDI

[?]

Lot or Batch Number: No
Serial Number: Yes
Expiration Date: No
Manufacturing Date: Yes
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: +4936715860
Email: SURGICAL@HILLROM.COM

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