FDA UDI In Commercial Distribution 🇺🇸 United States

Aliquot

DI: 00808232001020 · Model: 2090-0501 · Stryker Corporation
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Aliquot
Primary DI
00808232001020
Version / Model
2090-0501
Catalog Number
2090-0501
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
edb84f4e-44a4-438a-ae4d-c16f26ff337f

Device Description

Syringe Delivery Kit

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
KIH DISPENSER, CEMENT
OAR Injector, vertebroplasty (does not contain cement)

GMDN Terms

Code Name
45253 Orthopaedic cement preparation/delivery kit

Identifiers

Type ID
Primary 00808232001020

Customer Contacts

Device Sizes

Type Value Unit Text
Length 10.0 Centimeter
Needle Gauge 11.0 Gauge

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
20 – 30 Degrees Celsius