FDA UDI In Commercial Distribution 🇺🇸 United States

nva

DI: 00814008020522 · Model: AL-2939T-1218 · NVISION BIOMEDICAL TECHNOLOGIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
nva
Primary DI
00814008020522
Version / Model
AL-2939T-1218
Company Name
NVISION BIOMEDICAL TECHNOLOGIES, INC.
Labeler DUNS
047486041
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-05-30
Public Version
5
Public Version Date
2020-01-20
Public Version Status
Update
Public Device Record Key
071308d4-5cda-44e2-a422-f0b622b494a8

Device Description

Instrument, Trial Large, Anterior Lumbar Interbody Fusion System (ALIF)

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
MDM Instrument, Manual, Surgical, General Use

GMDN Terms

Code Name
32873 Surgical tamp, reusable

Identifiers

Type ID
Primary 00814008020522

Customer Contacts

Phone
210-545-3713

Device Sizes

Type Value Unit Text
Width 39 Millimeter
Length 29 Millimeter
Angle 12 degree
Height 18 Millimeter