FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 07613153000549 · Model: 5300010714 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
NA
Primary DI
07613153000549
Version / Model
5300010714
Catalog Number
5300-010-714
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
2022-02-16
Public Version Status
Update
Public Device Record Key
25c4dc09-5b9f-4d22-9aed-dff9c079071b

Device Description

2.0mm Tapered Side Cutting Solid Carbide Bur Medium

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
GFF BUR, SURGICAL, GENERAL & PLASTIC SURGERY

GMDN Terms

Code Name
45553 Orthopaedic bur, single-use

Identifiers

Type ID
Primary 07613153000549

Customer Contacts

Device Sizes

Type Value Unit Text
Length 50.8 Millimeter
Device Size Text, specify Diameter: 2.0 Millimeter