FDA UDI In Commercial Distribution 🇺🇸 United States

NuFix II

DI: B946021000010 · Model: IR · Nutech Spine, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NuFix II
Primary DI
B946021000010
Version / Model
IR
Catalog Number
02.100.001
Company Name
Nutech Spine, Inc.
Labeler DUNS
080867996
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-24
Public Version
2
Public Version Date
2023-04-21
Public Version Status
Update
Public Device Record Key
4484741c-b910-410d-a1d0-48c4d11836ac

Device Description

NuFix II Go/No-Go Gage

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
32845 Surgical depth gauge, reusable

Identifiers

Type ID
Primary B946021000010