FDA UDI Not in Commercial Distribution 🇺🇸 United States

VitaPrep

DI: 00808232001242 · Model: 2113-0013 · Stryker Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
VitaPrep
Primary DI
00808232001242
Version / Model
2113-0013
Catalog Number
2113-0013
Company Name
Stryker Corporation
Labeler DUNS
149183167
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-24
Public Version
3
Public Version Date
2019-04-23
Public Version Status
Update
Public Device Record Key
d6aa766b-49d9-4310-8f8b-1cd79d10d1c2
Distribution End Date
2018-06-30

Device Description

Plasma Separator

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
Yes
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LMF Agent, absorbable hemostatic, collagen based

GMDN Terms

Code Name
45669 Blood centrifugation system containment kit

Identifiers

Type ID
Package 30808232001243
Primary 00808232001242

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P050044 019
P050044 026

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
20 – 30 Degrees Celsius