AccessGUDID - DEVICE: Moog Medical Infinity Pole Clamp (30814844000086)

GUDID

Device Identifier (DI) Information

Brand Name: Moog Medical Infinity Pole Clamp
Version or Model: Infinity Pole Clamp, Multi pack
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 50741
Company Name: ZEVEX INTERNATIONAL, INC.

Primary DI Number: 30814844000086
Issuing Agency: GS1
Commercial Distribution End Date: November 03, 2021
Device Count: 5
Labeler D-U-N-S® Number*: 612746933 *Terms of Use

Device Description: Enteralite Infinity Pole Clamp

Device Characteristics

What MRI safety information does the labeling contain?	MR Unsafe
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?
41893	Medical device service rail clamp	A clamp designed to fit onto a medical device mounting rail or medical device service rail system to provide a secure method of fixing/mounting (holding) other medical or non-medical devices being used in the vicinity for patient treatment/care. It will typically be used in a hospital ward, a treatment room or an intensive care unit (ICU). It will have a gripping profile that is compatible to the medical rail it is intended to fit and a locking mechanism providing extra safety against inadvertent loosening. To this clamp, other adaptors may be fitted/slotted to provide holders for the devices to be carried, or it may have a dedicated function for which it is solely designed.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LZH	Pump, Infusion, Enteral

FDA Premarket Submission

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

Device Exempt from Premarket Submission: No 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: d6f24dea-e6ad-4b26-b5a6-71a93a3442ac
Public Version Date: November 11, 2021
Public Version Number: 1
DI Record Publish Date: November 03, 2021