FDA UDI In Commercial Distribution 🇺🇸 United States

EasyTouch

DI: MHC18023091 · Model: 802309 · MHC MEDICAL PRODUCTS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
EasyTouch
Primary DI
MHC18023091
Version / Model
802309
Company Name
MHC MEDICAL PRODUCTS, LLC
Labeler DUNS
169895245
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-02
Public Version
4
Public Version Date
2019-10-23
Public Version Status
Update
Public Device Record Key
8ffa6ec1-aacf-4d41-bbc6-14069b9f63f4

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
FMI Needle, Hypodermic, Single Lumen

GMDN Terms

Code Name
59230 Hypodermic needle, single-use

Identifiers

Type ID
Package MHC18023092
Primary MHC18023091