FDA UDI In Commercial Distribution 🇺🇸 United States

Vu cPOD

DI: 10889981106928 · Model: 11-40-0208 · Seaspine Orthopedics Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Vu cPOD
Primary DI
10889981106928
Version / Model
11-40-0208
Catalog Number
11-40-0208
Company Name
Seaspine Orthopedics Corporation
Labeler DUNS
079840876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-03
Public Version
6
Public Version Date
2025-10-24
Public Version Status
Update
Public Device Record Key
c4d8cd64-3c95-402d-a433-60727f57f26c

Device Description

Rasp 8mm Tapered

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
No
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
HTR RASP

GMDN Terms

Code Name
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Primary 10889981106928

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 8mm