FDA UDI In Commercial Distribution 🇺🇸 United States

Dermapac, Inc.

DI: 10810102270334 · Model: 5139 · Dermapac Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

Basic Information

Brand Name
Dermapac, Inc.
Primary DI
10810102270334
Version / Model
5139
Company Name
Dermapac Inc.
Labeler DUNS
796088466
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2022-09-12
Public Version
1
Public Version Date
2022-09-20
Public Version Status
New
Public Device Record Key
49dc0d7e-84f7-48b9-905f-7dc8daeed6d8

Device Description

OR/OB Gauze Packing 1"x108" stitched along 3 sides 8-ply NON x-ray

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
GDY Gauze/Sponge, Internal, X-Ray Detectable

GMDN Terms

Code Name
44971 General-purpose surgical sponge

Identifiers

Type ID
Unit of Use 00810102270337
Primary 10810102270334

Customer Contacts

Phone
203-924-7148