FDA UDI In Commercial Distribution 🇺🇸 United States

KM NEEDLE

DI: 18800020500660 · Model: KMS BE03530201 · K. M. S
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
100

Basic Information

Brand Name
KM NEEDLE
Primary DI
18800020500660
Version / Model
KMS BE03530201
Company Name
K. M. S
Labeler DUNS
689846211
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2019-07-21
Public Version
1
Public Version Date
2019-07-29
Public Version Status
New
Public Device Record Key
dd527bc3-7768-4ca1-bfa3-1c28450ba442

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
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MQX Needle, Acupuncture, Single Use

GMDN Terms

Code Name
34175 Acupuncture needle, single-use

Identifiers

Type ID
Package 38800020500664
Package 28800020500667
Primary 18800020500660
Unit of Use 08800020500663