FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 04546540030481 · Model: 1608002103 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
04546540030481
Version / Model
1608002103
Catalog Number
1608-002-103
Company Name
STRYKER CORPORATION
Labeler DUNS
196548481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-23
Public Version
2
Public Version Date
2022-02-22
Public Version Status
Update
Public Device Record Key
3b21b62d-f9d7-4bb8-8f7b-baf045f2d560

Device Description

2.4mm Heliocoidal Rasp

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
HWE INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT

GMDN Terms

Code Name
45553 Orthopaedic bur, single-use

Identifiers

Type ID
Primary 04546540030481

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Diameter: 2.4 Millimeter