FDA UDI In Commercial Distribution 🇺🇸 United States

Dermatec Viper Latex

DI: 00813417020376 · Model: GL+500BLACKPF · Relda, Llc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Dermatec Viper Latex
Primary DI
00813417020376
Version / Model
GL+500BLACKPF
Catalog Number
GL+500BLACKPF
Company Name
Relda, Llc.
Labeler DUNS
101926900
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2022-09-05
Public Version
1
Public Version Date
2022-09-13
Public Version Status
New
Public Device Record Key
888fd8fa-dc26-40a8-af99-0b40a9f02564

Device Description

Dermatec Viper Black latex PF exam glove xsmall 100/box, 10 box/case

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LYY Latex Patient Examination Glove

GMDN Terms

Code Name
47172 Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial

Identifiers

Type ID
Package 10813417020373
Primary 00813417020376
Unit of Use 70813417020375

Customer Contacts