FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 07613252170525 · Model: 0306808000 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613252170525
Version / Model
0306808000
Catalog Number
0306-808-000
Company Name
STRYKER CORPORATION
Labeler DUNS
196548481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-24
Public Version
3
Public Version Date
2021-09-20
Public Version Status
Update
Public Device Record Key
24b57b1f-2d35-451b-90bf-11b8111cf237

Device Description

Hand Drill

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
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
NDN CEMENT, BONE, VERTEBROPLASTY

GMDN Terms

Code Name
36235 Manual surgical rotary handpiece, reusable

Identifiers

Type ID
Package 37613252170526
Primary 07613252170525

Customer Contacts

Device Sizes

Type Value Unit Text
Needle Gauge 8.0 Gauge