FDA UDI In Commercial Distribution 🇺🇸 United States

NuTech Spine

DI: B946008010040 · Model: IR · Nutech Spine, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NuTech Spine
Primary DI
B946008010040
Version / Model
IR
Catalog Number
00.801.004
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
44ceb07c-b635-4c45-8bab-c37b350d837d

Device Description

Handle-Teardrop, Cannulated, LG Hudson (Fixed)

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
47829 Surgical instrument handle, non-torque-limiting

Identifiers

Type ID
Primary B946008010040