FDA UDI In Commercial Distribution 🇺🇸 United States

Aliquot

DI: 00808232001150 · Model: 2110-0513 · Stryker Corporation
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Aliquot
Primary DI
00808232001150
Version / Model
2110-0513
Catalog Number
2110-0513
Company Name
Stryker Corporation
Labeler DUNS
149183167
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-20
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
e9f1b259-6eb0-4b2b-9116-c55c29cfadf6

Device Description

Side-Port Syringe

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
Yes
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
OAR Injector, vertebroplasty (does not contain cement)
KIH DISPENSER, CEMENT

GMDN Terms

Code Name
45253 Orthopaedic cement preparation/delivery kit

Identifiers

Type ID
Primary 00808232001150

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Total Volume: 1.0 Cubic Centimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
20 – 30 Degrees Celsius