FDA UDI In Commercial Distribution 🇺🇸 United States

AnyPlus®

DI: 08806395440795 · Model: GS136-3710 · GS Medical Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AnyPlus®
Primary DI
08806395440795
Version / Model
GS136-3710
Catalog Number
GS136-3710
Company Name
GS Medical Co., Ltd.
Labeler DUNS
688385418
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-22
Public Version
1
Public Version Date
2020-09-30
Public Version Status
New
Public Device Record Key
63b1d5dc-b03e-4b08-bd8e-8ce736e99961

Device Description

Cervical Rasp,

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
Yes
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
HTR Rasp

GMDN Terms

Code Name
31335 Bone curette, reusable

Identifiers

Type ID
Primary 08806395440795

Customer Contacts

Phone
+82432377393