AccessGUDID - DEVICE: HOSE SET, ADVANCE CONTROL PADS (00842430104480)

GUDID

Device Identifier (DI) Information

Brand Name: HOSE SET, ADVANCE CONTROL PADS
Version or Model: 5996-35
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 5996-12
Company Name: MIZUHO ORTHOPEDIC SYSTEMS, INC.

Primary DI Number: 00842430104480
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 084527241 *Terms of Use

Device Description: No description.

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):	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?
62671	External cuff/pad inflation tubing set, single-use	A collection of devices consisting of flexible tubes and connectors, which may also include supportive devices (e.g., clamp), intended to be used to deliver air from a pump to a noninvasive, patient-contact pad, pack, cuff, or cushion. It may be intended for use with a specific type of assembly. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
CCX	Support, Patient Position

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: 9f58d25f-ab05-4547-b13e-80090ff2d98f
Public Version Date: September 24, 2021
Public Version Number: 3
DI Record Publish Date: August 05, 2019