FDA UDI Not in Commercial Distribution 🇺🇸 United States

Rite Aid Pharmacy

DI: 00011822096973 · Model: Family Planning Pregnancy Test One Step · SPD SWISS PRECISION DIAGNOSTICS GMBH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Rite Aid Pharmacy
Primary DI
00011822096973
Version / Model
Family Planning Pregnancy Test One Step
Company Name
SPD SWISS PRECISION DIAGNOSTICS GMBH
Labeler DUNS
483609579
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-24
Public Version
5
Public Version Date
2023-07-06
Public Version Status
Update
Public Device Record Key
c7cc095a-2918-43fb-9177-643331fe2fd0
Distribution End Date
2021-02-11

Device Description

FPPL Rite Aid SPS +/- (ER)

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
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
LCX Kit, Test, Pregnancy, Hcg, Over The Counter

GMDN Terms

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

Identifiers

Type ID
Primary 00011822096973
Package 10011822096970

Customer Contacts

Phone
800-899-7353

Premarket Submissions

Submission Number Supplement Number
K042280 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 30 Degrees Celsius