FDA UDI In Commercial Distribution 🇺🇸 United States

Biotem

DI: 08800036212611 · Model: AAAT50415B · Biotem Co., ltd
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Biotem
Primary DI
08800036212611
Version / Model
AAAT50415B
Company Name
Biotem Co., ltd
Labeler DUNS
557793214
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-31
Public Version
2
Public Version Date
2018-07-06
Public Version Status
New
Public Device Record Key
241dd0a5-9314-415a-8822-00cf4f99f3b0

Device Description

BIOTEM AR ANGLED ABUTMENT(HEX) 5.0mm Ⅹ 4mm(cuff) Ⅹ15'(angle)

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
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
No
Sterilization Prior Use
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
NHA Abutment, Implant, Dental, Endosseous

GMDN Terms

Code Name
55847 Dental implant system

Identifiers

Type ID
Primary 08800036212611

Premarket Submissions

Submission Number Supplement Number
K171297 000