AccessGUDID - DEVICE: Fisherbrand (00613647028698)

GUDID

Device Identifier (DI) Information

Brand Name: Fisherbrand
Version or Model: 13-711-5AMMD
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 137115AMMD
Company Name: FISHER SCIENTIFIC COMPANY L.L.C.

Primary DI Number: 00613647028698
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 500
Labeler D-U-N-S® Number*: 004321519 *Terms of Use

Device Description: FB TRANSFER PIPETTE 5ML

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?
43375	User-induced pipette	A device designed for the manual withdrawal, transfer, and injection of small volumes of fluid materials. It is made of glass or plastic and is designed as a long thin tube, typically with graduations along its length. The user will typically attach a mouthpiece and create a partial vacuum within the pipette by gently sucking the air from inside the tube inducing the liquid to enter the pipette, or achieve the same action with a squeezable bulb. Closing the mouthpiece or the user end of the pipette will hold the liquid therein; dispensing is done by controlled venting of air into the user end or squeezing the bulb.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
JRC	MICRO PIPETTE

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: f5c3913e-e20c-42b0-9dd6-659502063db5
Public Version Date: July 08, 2025
Public Version Number: 1
DI Record Publish Date: June 30, 2025