FDA UDI In Commercial Distribution 🇺🇸 United States

Fortis ACP

DI: 08800039828857 · Model: A · DIOMEDICAL CO.,LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Fortis ACP
Primary DI
08800039828857
Version / Model
A
Catalog Number
TP.VDA.4014
Company Name
DIOMEDICAL CO.,LTD.
Labeler DUNS
557795909
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-07-19
Public Version
2
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
222ebd0d-e8ae-47f9-8885-7d11e511daa2

Device Description

Variable-angle screws (self-drilling) D4 x L14

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
KWQ Appliance, fixation, spinal intervertebral body

GMDN Terms

Code Name
56642 Orthopaedic bone screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary 08800039828857

Customer Contacts

Phone
+82313699470 ext. 112

Premarket Submissions

Submission Number Supplement Number
K173099 000