FDA UDI In Commercial Distribution 🇺🇸 United States

Globe

DI: 00850026393064 · Model: 20202 · Trifecta Pharmaceuticals USA LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
100

Basic Information

Brand Name
Globe
Primary DI
00850026393064
Version / Model
20202
Company Name
Trifecta Pharmaceuticals USA LLC
Labeler DUNS
079424163
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2021-02-28
Public Version
2
Public Version Date
2021-08-24
Public Version Status
Update
Public Device Record Key
58c6e431-74c8-4e14-b1bf-185c55a1931c

Device Description

Globe Sterile Gauze Pads 3 x 3 Box of 100

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NAB Gauze / Sponge,Nonresorbable For External Use

GMDN Terms

Code Name
48134 Woven gauze pad

Identifiers

Type ID
Unit of Use 00850026393019
Primary 00850026393064

Customer Contacts

Phone
888-296-9067