Curaplex

Basic Information

• Brand Name: Curaplex
• Primary DI: 00812574026412
• Version / Model: 301-PFR9WN
• Company Name: TRI-ANIM HEALTH SERVICES, INC.
• Labeler DUNS: 010712461
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2017-02-06
• Public Version: 3
• Public Version Date: 2018-07-06
• Public Version Status: Update
• Public Device Record Key: 5c94a71a-e3cb-40e2-bc1c-8ec1ba957643

Device Description

FILTER,N/C,27.0 ID,30.1OD

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): Yes
• Over the Counter (OTC): No
• Kit: Yes
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: Yes
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: No
• Has Serial Number: Yes
• Has Lot/Batch Number: No
• 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
BZG	SPIROMETER, DIAGNOSTIC	Anesthesiology	868.1840	2

GMDN Terms

Code	Name	Definition	Implantable	Status
60506	Pulmonary function testing kit	A collection of non-sterile devices intended to be used in conjunction with pulmonary function analysis equipment to perform a pulmonary function test. It may include a breathing mouthpiece, filter (intended to reduce contamination of parent device), and a nose clip. This is a single-use device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Package	00812574026764	GS1		100	In Commercial Distribution
Primary	00812574026412	GS1

Premarket Submissions

Submission Number	Supplement Number
K042758	000

Device Sizes

Type	Value	Unit	Text
Lumen/Inner Diameter	25.4	Millimeter