AccessGUDID - DEVICE: Adaptive Cylindrical Cuff, Limited Reuse (M995995000421)

GUDID

Device Identifier (DI) Information

Brand Name: Adaptive Cylindrical Cuff, Limited Reuse
Version or Model: 9-9500-042
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: Delfi Medical Innovations Inc

Primary DI Number: M995995000421
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 251078945 *Terms of Use

Device Description: Delfi Adaptive Tourniquet Cuffs are available in a selection of lengths to facilitate a proper fit, and color coded for size identification. Each Delfi Adaptive Tourniquet Cuff includes a single use Matching Limb Protection Sleeve. Delfi Adaptive Tourniquet Cuffs are provided sterile, and may be reused in a non-sterile manner for up to five uses. Delfi Adaptive Tourniquet Cuffs are not designed to be resterilized. Dispose of properly after use.

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?
35925	Tourniquet cuff, single-use	A band-like device that is applied around an extremity (arm or leg) and connected to a tourniquet unit to apply a controlled pressure to restrict blood circulation and prevent normal blood flow to or from the distal area during a surgical intervention or serious injury. The tourniquet unit is used to provide the pressure within the cuff and display the pressure applied. The cuff usually comprises a dual-chamber allowing for alternation of the pressure site to avoid tissue damage or necrosis. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
KCY	Tourniquet, Pneumatic

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: c96201b5-b6b7-4a5b-ab03-72a6b29f625f
Public Version Date: January 16, 2026
Public Version Number: 1
DI Record Publish Date: January 08, 2026