AccessGUDID - DEVICE: MEDLINE INDUSTRIES, INC. (10080196820764)

GUDID

Device Identifier (DI) Information

Brand Name: MEDLINE INDUSTRIES, INC.
Version or Model: DYNJ04230
Commercial Distribution Status: In Commercial Distribution
Catalog Number: DYNJ04230
Company Name: MEDLINE INDUSTRIES, INC.

Primary DI Number: 10080196820764
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 025460908 *Terms of Use

Device Description: HOOK,AMNIO,PLASTIC,STERILE

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):	Yes
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?
63417	Low-pressure tubing connector, single-use, sterile	A sterile device designed to connect together two or more tubes typically with the intention of creating an extension. The connecting ends of this device will typically be serrated to provide a secure grip for the applied tubes. Clips or other forms of locking devices may be applied over the tubes to further secure the fitting. This device will not be appropriate for connecting tubes that are designed to carry (withstand) high pressures [e.g., high pressure gases]. This is a single-use device.	Obsolete	false

FDA Product Code

[?]

Product Code	Product Code Name
HHF	REMOVER, INTRAUTERINE DEVICE, CONTRACEPTIVE, HOOK-TYPE

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: cc8c3be0-8191-4e35-999a-182ac0897cf2
Public Version Date: January 08, 2021
Public Version Number: 1
DI Record Publish Date: December 31, 2020