AccessGUDID - DEVICE: Advocate Syringes for U-100 Insulin 30G .3CC 5/16" Needle (00894046001806)

GUDID

Device Identifier (DI) Information

Brand Name: Advocate Syringes for U-100 Insulin 30G .3CC 5/16" Needle
Version or Model: 607
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 607S
Company Name: DIABETIC SUPPLY OF SUNCOAST, INC.

Primary DI Number: 00894046001806
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 10
Labeler D-U-N-S® Number*: 043081723 *Terms of Use

Device Description: Advocate Syringes for U-100 Insulin 30G .3CC 5/16" Needle, Single Use, Sleeve of 10

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):	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?
35904	Metered-delivery hypodermic syringe	A sterile device consisting of a graduated barrel (cylinder) with plunger intended to be used to deliver (inject) or withdraw an accurate metered dose of a fluid to/from the body. The application of the content of this device may be in conjunction with an injector device (transcutaneous delivery) or through the traditional use of a needle (subcutaneous delivery). It may allow for retraction of an attached needle (safety syringe); the needle is not included. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FMF	Syringe, Piston

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: 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: 2fc5363b-53fc-41be-9ce0-574f284f8309
Public Version Date: February 07, 2022
Public Version Number: 7
DI Record Publish Date: August 20, 2016