Device
032-10-301U
Manufacturer
ENCHANT TEK. CO, LTD.
Model: 032-10-301U Catalog: 032-10-301U DI: 04719882305610 Status: New MRI: Labeling does not contain MRI Safety Information Single-use: No Rx: Yes OTC: No
First Published: 2026-05-28 Current Version: 2026-06-05
Sterilization
Device Sterile: No
Sterilization Prior To Use: No
Regulatory & Distribution
Record Status: Published
Version Number: 1
Record Key: 8f8d1f0a-992d-4176-ba40-ec2d0cbdad61
Distribution Status: In Commercial Distribution
DUNS Number: 656173001
Device Count: 1
DM Exempt: No
Premarket Exempt: No
HCT/P: No
Kit: No
Combination Product: No
Lot/Batch Tracked: Yes
Serial Number Tracked: No
Manufacturing Date Tracked: Yes
Expiration Date Tracked: Yes
Donation ID Number Tracked: No
Labeled Contains NRL: No
Labeled No NRL: No
Identifiers
Item #1 - Pkg Type: BOX
Item #1 - Device ID: 14719882305617
Item #1 - Pkg Status: In Commercial Distribution
Item #1 - Pkg Quantity: 10
Item #1 - Device ID Type: Package
Item #1 - Contains DINumber: 04719882305610
Item #1 - Device ID Issuing Agency: GS1
Item #2 - Device ID: 04719882305610
Item #2 - Device ID Type: Primary
Item #2 - Device ID Issuing Agency: GS1
Item #3 - Pkg Type: carton
Item #3 - Device ID: 24719882305614
Item #3 - Pkg Status: In Commercial Distribution
Item #3 - Pkg Quantity: 60
Item #3 - Device ID Type: Package
Item #3 - Contains DINumber: 14719882305617
Item #3 - Device ID Issuing Agency: GS1
GMDN
Code: 31266
Name: Incentive spirometer
Definition:
A hand-held, mechanical, breathing-muscle exerciser intended to be used in respiratory therapy to encourage and motivate deep-breathing manoeuvres, typically for the postsurgical treatment and prevention of atelectasis (lung collapse) and to help facilitate airway opening and clearing. It includes an indicator in a housing that rises in relation to patient inspiratory effort, performed via an attached tube and mouthpiece, to determine the maximum volume of gas which can be inspired [i.e., the inspiratory vital capacity (IVC)]. This is a single-patient device designed for use in a medical facility and in the home. This is a reusable device.
FDA Product Codes
BWF
Spirometer, Therapeutic (Incentive)
Premarket Submissions
Submission Number: K233855
Supplement Number: 000