FDA UDI In Commercial Distribution 🇺🇸 United States

IMMULITE®/IMMULITE®1000 Systems AF AFP

DI: 00630414963594 · Model: 10381162 · SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
IMMULITE®/IMMULITE®1000 Systems AF AFP
Primary DI
00630414963594
Version / Model
10381162
Catalog Number
LKAP1
Company Name
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD
Labeler DUNS
296822794
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-24
Public Version
5
Public Version Date
2021-11-18
Public Version Status
Update
Public Device Record Key
ae07d37a-690c-4a0f-8c3b-3cd8bd3307ed

Device Description

AF AFP Kit 100 Test

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
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
LOK Kit, Test, Alpha-Fetoprotein For Neural Tube Defects

GMDN Terms

Code Name
58348 Alpha-fetoprotein (AFP) IVD, kit, chemiluminescent immunoassay

Identifiers

Type ID
Primary 00630414963594

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P010007 001
P010007 002
P010007 004
P010007 005

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Protect from Light
Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius