FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 10886982070159 · Model: 03.025.136 · SYNTHES (U.S.A.) LP
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886982070159
Version / Model
03.025.136
Catalog Number
03025136
Company Name
SYNTHES (U.S.A.) LP
Labeler DUNS
832637081
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-31
Public Version
7
Public Version Date
2023-10-04
Public Version Status
Update
Public Device Record Key
56fe8af9-5a4a-4635-9d34-103ecb18bd13
Distribution End Date
2020-07-26

Device Description

4.9MM/7.0MM DRILL-REAMER QC/288MM FOR 6.0MM ASLS

Device Characteristics

Single Use
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HTO REAMER

GMDN Terms

Code Name
45114 Bone-resection orthopaedic reamer, reusable

Identifiers

Type ID
Direct Marking 07611819865976
Secondary H679030251360
Primary 10886982070159

Customer Contacts