FDA UDI Not in Commercial Distribution 🇺🇸 United States

Kelyniam CSI

DI: 00817580025367 · Model: PEEK-IM1001 · KELYNIAM GLOBAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Kelyniam CSI
Primary DI
00817580025367
Version / Model
PEEK-IM1001
Catalog Number
PEEK-IM1001
Company Name
KELYNIAM GLOBAL, INC.
Labeler DUNS
785088829
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-20
Public Version
1
Public Version Date
2020-04-28
Public Version Status
New
Public Device Record Key
8c71e035-a9e3-4233-ac5e-004d7ae2f510
Distribution End Date
2020-04-20

Device Description

PEEK Customized Cranial Implant, Small CSI092419-DR1

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
Yes
MRI Safety
MR Safe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
Yes

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
GXN Plate, Cranioplasty, Preformed, Non-Alterable

GMDN Terms

Code Name
46268 Cranioplasty plate, non-alterable

Identifiers

Type ID
Primary 00817580025367

Premarket Submissions

Submission Number Supplement Number
K103582 000