FDA UDI In Commercial Distribution 🇺🇸 United States

Ultragard

DI: 00816928021320 · Model: V300-M · Ultragard
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Ultragard
Primary DI
00816928021320
Version / Model
V300-M
Company Name
Ultragard
Labeler DUNS
175840941
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-02-03
Public Version
1
Public Version Date
2025-02-11
Public Version Status
New
Public Device Record Key
6dfd3833-a7ba-4ed5-a10c-f5dd1e29fc38

Device Description

box of 100 powder free vinyl examination gloves, non-sterile, size Medium

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
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LYZ Vinyl Patient Examination Glove

GMDN Terms

Code Name
47176 Vinyl examination/treatment glove, non-powdered

Identifiers

Type ID
Package 00816928026325
Primary 00816928021320