FDA UDI In Commercial Distribution 🇺🇸 United States

DIOnavi. Anchor sleeve

DI: 08800049407523 · Model: AS 20_50 · DIO Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

Basic Information

Brand Name
DIOnavi. Anchor sleeve
Primary DI
08800049407523
Version / Model
AS 20_50
Company Name
DIO Corporation
Labeler DUNS
631085206
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2022-12-01
Public Version
1
Public Version Date
2022-12-09
Public Version Status
New
Public Device Record Key
40a48b5d-58b3-4d5c-bad6-806f14656f94

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
Yes
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
NDP Accessories, Implant, Dental, Endosseous

GMDN Terms

Code Name
64371 Dental implantation drilling template guide-sleeve

Identifiers

Type ID
Unit of Use 08800049300220
Primary 08800049407523