FDA UDI In Commercial Distribution 🇺🇸 United States

HydroSet XT

DI: 07613327064285 · Model: 897010 · Stryker Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HydroSet XT
Primary DI
07613327064285
Version / Model
897010
Catalog Number
897010
Company Name
Stryker Corporation
Labeler DUNS
149183167
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-03-21
Public Version
3
Public Version Date
2019-02-07
Public Version Status
Update
Public Device Record Key
12999cd8-1b84-4c37-949a-0909b29b1380

Device Description

Injectable HA Bone Cement

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
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MQV FILLER, BONE VOID, CALCIUM COMPOUND

GMDN Terms

Code Name
47997 Bone grafting cannula

Identifiers

Type ID
Primary 07613327064285

Device Sizes

Type Value Unit Text
Device Size Text, specify Total Volume: 10.0 Cubic Centimeter

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
15 – 25 Degrees Celsius