FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10887587008752 · Model: 03.000.130S · SYNTHES (U.S.A.) LP
Product Codes
4
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10887587008752
Version / Model
03.000.130S
Catalog Number
03000130S
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
a814fb4e-b0de-4727-9109-bc9c4ca5cc7f

Device Description

BURR PIN-SHAPED S Ø 2.1MM HEAD LENGTH 12MM

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

GMDN Terms

Code Name
36249 Orthopaedic bur, reusable

Identifiers

Type ID
Secondary H98003000130S0
Primary 10887587008752

Premarket Submissions

Submission Number Supplement Number
K043310 000