FDA UDI In Commercial Distribution 🇺🇸 United States

Precision

DI: 00887868463327 · Model: 110009769 · Biomet Orthopedics, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Precision
Primary DI
00887868463327
Version / Model
110009769
Catalog Number
110009769
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-23
Public Version
2
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
2839d19f-ce38-4a0e-916c-073de6dedf5d

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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
46165 Orthopaedic guidewire, reusable

Identifiers

Type ID
Primary 00887868463327

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 2.1 mm 17"