FDA UDI In Commercial Distribution 🇺🇸 United States

IVA Cage

DI: 08800039825610 · Model: A · DIOMEDICAL CO.,LTD.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
IVA Cage
Primary DI
08800039825610
Version / Model
A
Catalog Number
TI.2239
Company Name
DIOMEDICAL CO.,LTD.
Labeler DUNS
557795909
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-14
Public Version
2
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
c7ce6f11-954f-4231-b609-fac1cfbe0e71

Device Description

TLIF BULLET TRIAL L32 x W9 x A8 x H15

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
MR Unsafe
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
MAX Intervertebral fusion device with bone graft, lumbar
ODP Intervertebral fusion device with bone graft, cervical

GMDN Terms

Code Name
46653 Spinal fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary 08800039825610

Customer Contacts

Phone
+82313699470 ext. 112

Premarket Submissions

Submission Number Supplement Number
K162220 000