FDA UDI In Commercial Distribution 🇺🇸 United States

Resistex

DI: 10641043370001 · Model: 10-37000 · MERCURY ENTERPRISES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Resistex
Primary DI
10641043370001
Version / Model
10-37000
Company Name
MERCURY ENTERPRISES, INC.
Labeler DUNS
032705659
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-03-02
Public Version
6
Public Version Date
2023-11-17
Public Version Status
Update
Public Device Record Key
72b17b66-2e7b-484e-9312-c321163f2fe3

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
BWF Spirometer, Therapeutic (Incentive)

GMDN Terms

Code Name
31266 Incentive spirometer

Identifiers

Type ID
Primary 10641043370001
Package 30641043370005

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K942919 000