FDA UDI In Commercial Distribution 🇺🇸 United States

COUNTERSINK

DI: 00887868067730 · Model: 939999252 · Biomet Orthopedics, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
COUNTERSINK
Primary DI
00887868067730
Version / Model
939999252
Catalog Number
939999252
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-23
Public Version
1
Public Version Date
2020-06-01
Public Version Status
New
Public Device Record Key
c90f642d-03e9-4cb6-8aa2-493b7f233b99

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
HWD STARTER, BONE SCREW

GMDN Terms

Code Name
16462 Surgical countersink, reusable

Identifiers

Type ID
Primary 00887868067730

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 3.5MM DIA.