AccessGUDID - DEVICE: Fisherbrand (00613647020623)

GUDID

Device Identifier (DI) Information

Brand Name: Fisherbrand
Version or Model: 19-010-411
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 19010411
Company Name: FISHER SCIENTIFIC COMPANY L.L.C.

Primary DI Number: 00613647020623
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 25
Labeler D-U-N-S® Number*: 004321519 *Terms of Use

Device Description: TRNIQTS NON-LTX BLUE 25/REEL

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?
58128	Limb tourniquet, manual, single-use	A strap or tubing intended to be wrapped around a patient's limb (arm or leg) and manually tightened to reduce blood circulation to or from the portion of the limb distal to where the device is applied. It is typically used by emergency medical services (EMS) for emergency blood loss prevention or for routine blood sampling. It typically does not include latex and may be available in a variety of designs (e.g., Velcro or a self-locking buckle, synthetic rubber band). This is a single-use device.	Obsolete	false

FDA Product Code

[?]

Product Code	Product Code Name
GAX	TOURNIQUET, NONPNEUMATIC

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: 27063cc0-28ba-44e3-ac62-6beee8b1d567
Public Version Date: December 07, 2022
Public Version Number: 1
DI Record Publish Date: November 29, 2022