FDA UDI In Commercial Distribution 🇺🇸 United States

GoldenDent

DI: 00850011211946 · Model: GO GKI · GoldenDent
Product Codes
1
GMDN Terms
9
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
GoldenDent
Primary DI
00850011211946
Version / Model
GO GKI
Catalog Number
GO GKI
Company Name
GoldenDent
Labeler DUNS
078273228
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-02-26
Public Version
2
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
7584c172-3f13-4c84-b1b9-7106a873ed02

Device Description

Grafting Instrument Kit (11 Instruments)

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
Combination Product
Yes
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
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
EKF Instrument, Contouring, Matrix, Operative

GMDN Terms

Code Name
35559 Bone file/rasp, manual, reusable
13502 Suture scissors
31335 Bone curette, reusable
12726 Suturing needle holder, reusable
62466 Surgical soft-tissue manipulation forceps, tweezers-like, reusable
41544 Periodontal knife
38168 Periosteal elevator, reusable
12235 Scalpel handle, reusable
45119 Dappen dish, reusable

Identifiers

Type ID
Primary 00850011211946