AccessGUDID - DEVICE: De Soutter Medical (05051471127487)

GUDID

Device Identifier (DI) Information

Brand Name: De Soutter Medical
Version or Model: P20-108
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: P20-108
Company Name: DE SOUTTER MEDICAL LIMITED

Primary DI Number: 05051471127487
Issuing Agency: GS1
Commercial Distribution End Date: November 01, 2024
Device Count: 1
Labeler D-U-N-S® Number*: 458064144 *Terms of Use

Device Description: ECO PULSE - H/P HIP ARTHROPLASTY PUMP KIT LESS SUCTION

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:	Yes
Prescription Use (Rx):	Yes
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?
47891	Surgical irrigation system nozzle	A surgically-invasive device designed to be attached to the distal end of a lavage system or kit handpiece to intraoperatively function as an applicator/nozzle that produces an intentional jet, stream or spray of sterile fluid (typically saline) from its aperture to the site of operation during a surgical intervention (e.g., trauma, soft tissue application and orthopaedic) for the purpose of removing tissue, bone debridement and/or bone cement residue, and to clean the site; it may in addition perform aspiration (suction). It is available in many designs (e.g., fan spray, built-in filter, splash shield, brush); however, it is not a single-hole cannula/tubing. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FQH	Lavage, Jet

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: Yes
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: 77d85528-cfcb-4650-8ac4-f0cc202a1e42
Public Version Date: November 01, 2024
Public Version Number: 6
DI Record Publish Date: January 17, 2018