FDA UDI In Commercial Distribution 🇺🇸 United States

nvc

DI: 00814008023240 · Model: AC-1000C-102 · NVISION BIOMEDICAL TECHNOLOGIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
nvc
Primary DI
00814008023240
Version / Model
AC-1000C-102
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
4
Public Version Date
2020-01-20
Public Version Status
Update
Public Device Record Key
8ae3550b-3291-4a1f-9da1-590e0a1e49c5

Device Description

Case Lid, Anterior Cervical Interbody Fusion System (ACIF)

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
42997 Surgical instrument/implant rack

Identifiers

Type ID
Primary 00814008023240

Customer Contacts

Phone
210-545-3713

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
should not exceed 25 lbs filled, should not be stacked