FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10887587009193 · Model: 03.000.220S · SYNTHES (U.S.A.) LP
Product Codes
4
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10887587009193
Version / Model
03.000.220S
Catalog Number
03000220S
Company Name
SYNTHES (U.S.A.) LP
Labeler DUNS
832637081
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-30
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
d19ed3dd-349d-4e37-ba30-a8cc9cced83b

Device Description

BURR TAPERED FISSURE LGTH 45MM Ø 2.1MM W/J-LATCH COUPLING

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
ERL DRILL, SURGICAL, ENT (ELECTRIC OR PNEUMATIC) INCLUDING HANDPIECE
DZI DRILL, BONE, POWERED
HBE DRILLS, BURRS, TREPHINES & ACCESSORIES (SIMPLE, POWERED)
HWE INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT

GMDN Terms

Code Name
36249 Orthopaedic bur, reusable

Identifiers

Type ID
Secondary H98003000220S0
Primary 10887587009193

Premarket Submissions

Submission Number Supplement Number
K043310 000