FDA UDI In Commercial Distribution 🇺🇸 United States

Dermatec Twilight

DI: 00813417020635 · Model: GL+601STNITRILE · Relda, Llc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Dermatec Twilight
Primary DI
00813417020635
Version / Model
GL+601STNITRILE
Catalog Number
GL+601STNITRILE
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
207c3cb7-7178-4b7d-b81c-cd84f4ff379e

Device Description

Dermatec Twilight Blue Stretch Nitrile PF exam glove medium 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
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
No
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

GMDN Terms

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

Identifiers

Type ID
Package 10813417020632
Primary 00813417020635
Unit of Use 70813417020634

Customer Contacts