FDA UDI In Commercial Distribution 🇺🇸 United States

REBORN Fixture

DI: 08800023152104 · Model: IC1M3511OC · Cybermed Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
REBORN Fixture
Primary DI
08800023152104
Version / Model
IC1M3511OC
Company Name
Cybermed Inc.
Labeler DUNS
688248447
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-10-31
Public Version
1
Public Version Date
2022-11-08
Public Version Status
New
Public Device Record Key
009a0b48-838a-4fce-bdc0-f9ff3d05eed6

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
Yes
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DZE Implant, Endosseous, Root-Form

GMDN Terms

Code Name
55849 Screw endosteal dental implant, two-piece

Identifiers

Type ID
Primary 08800023152104

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K210039 000