FDA UDI In Commercial Distribution 🇺🇸 United States

BioStrip® P

DI: 10743816000754 · Model: BXI-113-50-01 · PRINCETON BIOMEDITECH CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BioStrip® P
Primary DI
10743816000754
Version / Model
BXI-113-50-01
Catalog Number
BXI-113-50-01
Company Name
PRINCETON BIOMEDITECH CORPORATION
Labeler DUNS
362917692
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
3
Public Version Date
2023-07-06
Public Version Status
Update
Public Device Record Key
ed59fb25-7e09-4f7f-8878-28893260e5c2

Device Description

BioStrip® P; 50 Test kit; CE

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DHA System, Test, Human Chorionic Gonadotropin

GMDN Terms

Code Name
33819 Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical

Identifiers

Type ID
Primary 10743816000754

Customer Contacts

Phone
7322741000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 30 Degrees Celsius