FDA UDI In Commercial Distribution 🇺🇸 United States

MICROFLEX

DI: 00769799220197 · Model: US-220-XL · Ansell Healthcare Product
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

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Basic Information

Brand Name
MICROFLEX
Primary DI
00769799220197
Version / Model
US-220-XL
Catalog Number
US-220-XL
Company Name
Ansell Healthcare Product
Labeler DUNS
111267330
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2022-03-14
Public Version
1
Public Version Date
2022-03-22
Public Version Status
New
Public Device Record Key
553dc7f7-2e80-4293-9754-349741584f58

Device Description

MICROFLEX US-220 ULTRASENSE SIZE XL (9.5-10.0), Nitrile Powder-Free Examination Glove

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LZA Polymer Patient Examination Glove
LZC Patient Examination Glove, Specialty

GMDN Terms

Code Name
56286 Nitrile examination/treatment glove, non-powdered, non-antimicrobial

Identifiers

Type ID
Package 00769799220098
Primary 00769799220197
Unit of Use 00071483004113

Customer Contacts

Phone
775-746-6600
Phone
775-470-7106