FDA UDI In Commercial Distribution 🇺🇸 United States

Pulse® CR Aqua

DI: 40813172023160 · Model: 194202 · INNOVATIVE HEALTHCARE CORPORATION
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
200

Basic Information

Brand Name
Pulse® CR Aqua
Primary DI
40813172023160
Version / Model
194202
Company Name
INNOVATIVE HEALTHCARE CORPORATION
Labeler DUNS
802020693
Distribution Status
In Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2022-12-08
Public Version
2
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
6e944d9b-4e7e-44f7-ace6-e7aaf62febdc

Device Description

Gloves, Exam, Chloroprene, Non-Sterile, Powder-Free, Textured, Aqua, M

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
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
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
OPC Powder-Free Polychloroprene Patient Examination Glove
LZC Patient Examination Glove, Specialty

GMDN Terms

Code Name
56288 Polychloroprene examination/treatment glove, non-powdered

Identifiers

Type ID
Package 30813172023163
Primary 40813172023160
Unit of Use 00813172023162