SoftCheck

Basic Information

• Brand Name: SoftCheck
• Primary DI: 00858293006571
• Version / Model: ST2635FL
• Company Name: REPROCESSING PRODUCTS CORPORATION
• Labeler DUNS: 796083392
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2019-08-30
• Public Version: 1
• Public Version Date: 2019-09-09
• Public Version Status: New
• Public Device Record Key: 4abc209b-4075-4bcd-8242-cf8b798aa3d5

Device Description

BP Cuff, Regular Adult, 26-35 cm, 1 Tube

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): No
• Over the Counter (OTC): No
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: No
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: No
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: No
• Has Expiration Date: No
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
DXQ	Blood Pressure Cuff	Cardiovascular	870.1120	2

GMDN Terms

Code	Name	Definition	Implantable	Status
37326	Blood pressure cuff, single-use	A band-like device that has an inflatable bladder in an inelastic sleeve with one or two connecting tubes with connector (typically locking connectors) that can be connected to a mechanism for inflating and deflating the bladder and/or a sphygmomanometer or a patient monitoring device/system that is used to determine a patient's blood pressure. It is typically wrapped around the upper arm of the patient. This is a single-use device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Package	10858293006578	GS1	Bag	5	In Commercial Distribution
Primary	00858293006571	GS1

Premarket Submissions

Submission Number	Supplement Number
K940214	000