FDA UDI In Commercial Distribution 🇺🇸 United States

Plastic Cylinder

DI: 08800049241820 · Model: API 48514N[H] · DIO Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Plastic Cylinder
Primary DI
08800049241820
Version / Model
API 48514N[H]
Company Name
DIO Corporation
Labeler DUNS
631085206
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-09-15
Public Version
1
Public Version Date
2025-09-23
Public Version Status
New
Public Device Record Key
f6639e54-b545-48f5-8081-48ec0dd96969

Device Characteristics

Single Use
Yes
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
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
DZE Implant, Endosseous, Root-Form

GMDN Terms

Code Name
44880 Dental implant suprastructure, temporary, preformed, single-use

Identifiers

Type ID
Primary 08800049241820

Premarket Submissions

Submission Number Supplement Number
K070569 000