FDA UDI In Commercial Distribution 🇺🇸 United States

METICULY Patient-specific titanium mesh implant

DI: 08859751216008 · Model: CP-300 · METICULY COMPANY LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
METICULY Patient-specific titanium mesh implant
Primary DI
08859751216008
Version / Model
CP-300
Company Name
METICULY COMPANY LIMITED
Labeler DUNS
661695214
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-03-05
Public Version
1
Public Version Date
2026-03-13
Public Version Status
New
Public Device Record Key
5771b5b1-fe99-4fd2-ad3d-bdc734ce8b2e

Device Description

METICULY Patient-specific titanium mesh implant (advanced design) non-sterile

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
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

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 08859751216008
Package 18859751216005