FDA UDI In Commercial Distribution 🇺🇸 United States

PremierPro

DI: 00818566016348 · Model: 6912 · PRESTIGE AMERITECH, LTD.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
PremierPro
Primary DI
00818566016348
Version / Model
6912
Company Name
PRESTIGE AMERITECH, LTD.
Labeler DUNS
199692794
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-01
Public Version
4
Public Version Date
2026-03-23
Public Version Status
Update
Public Device Record Key
09adf529-b52c-49ab-8abe-e461d71317c8

Device Description

Seracult Fecal Occult Blood Test, Triple Slide Patient Kit

Device Characteristics

Single Use
No
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
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
KHE Reagent, Occult Blood

GMDN Terms

Code Name
54531 Faecal occult blood IVD, kit, rapid colorimetric, clinical

Identifiers

Type ID
Package 10818566016345
Primary 00818566016348

Customer Contacts