FDA UDI In Commercial Distribution 🇺🇸 United States

Phadia 100

DI: 07333066000992 · Model: 12-3500-02 · Phadia AB
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Phadia 100
Primary DI
07333066000992
Version / Model
12-3500-02
Catalog Number
12-3500-02
Company Name
Phadia AB
Labeler DUNS
354019424
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
4
Public Version Date
2022-09-16
Public Version Status
Update
Public Device Record Key
d8e1f31b-a65c-426e-8601-4300d26f6ce5

Device Description

Phadia 100

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
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
Yes
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
DHB SYSTEM, TEST, RADIOALLERGOSORBENT (RAST) IMMUNOLOGICAL

GMDN Terms

Code Name
56705 Fluorescent immunoassay analyser IVD, laboratory

Identifiers

Type ID
Primary 07333066000992

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K051218 000