FDA UDI In Commercial Distribution 🇺🇸 United States

Spinal System

DI: 00880304837232 · Model: 132M2350 · BIOMET SPINE LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Spinal System
Primary DI
00880304837232
Version / Model
132M2350
Catalog Number
132M2350
Company Name
BIOMET SPINE LLC
Labeler DUNS
018577570
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-07-13
Public Version
3
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
2de2231d-4240-42be-b681-458c2463dc0e

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
HTF CURETTE

GMDN Terms

Code Name
31335 Bone curette, reusable

Identifiers

Type ID
Primary 00880304837232

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Micro Curette 75° Down 5.0 mm