FDA UDI In Commercial Distribution 🇺🇸 United States

Aliquot

DI: 00808232001211 · Model: 2110-0530 · Stryker Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Aliquot
Primary DI
00808232001211
Version / Model
2110-0530
Catalog Number
2110-0530
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
3
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
2c4aed1b-6c60-4f47-a19d-9c4e61fb260e

Device Description

Directional Bone Tamp

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
No
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
OCJ spinal channeling instrument, vertebroplasty

GMDN Terms

Code Name
47022 Neurosurgical curette, single-use

Identifiers

Type ID
Primary 00808232001211

Customer Contacts

Device Sizes

Type Value Unit Text
Needle Gauge 14.0 Gauge
Length 6.0 Inch

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
20 – 30 Degrees Celsius