AccessGUDID - DEVICE: Medi-Rip 3" (00347682631017)

GUDID

Device Identifier (DI) Information

Brand Name: Medi-Rip 3"
Version or Model: 63101
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 63101
Company Name: Medique Products

Primary DI Number: 00347682631017
Issuing Agency: GS1
Commercial Distribution End Date: July 15, 2019
Device Count: 1
Labeler D-U-N-S® Number*: 086911794 *Terms of Use

Device Description: An elastic bandage device consisting of a long flat strip of elasticized non-latex cohesive material that is used as a wrap to support and compress a part of a patient's body.

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":	Yes
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?
13369	Skin treatment/dressing-supportive limb/finger bandage, single-use	An elastic, tubular device intended to be worn over/around the limb (arm/leg) and/or finger of a patient affected by a skin condition/disorder (e.g., eczema, wound, fragile skin) to protect the skin typically after treatment with a medication (e.g., ointment, cream), and/or to support a dressing over a wound/injury; it is not designed for tissue support/compression. It is typically made of non-allergenic natural materials or a composite (e.g., viscose/nylon/elastane), and intended for use in the home and healthcare facility. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FQM	Bandage, Elastic

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: dcd10c72-0598-4a68-9f98-cd617872f546
Public Version Date: September 20, 2021
Public Version Number: 2
DI Record Publish Date: July 12, 2019