FDA UDI In Commercial Distribution 🇺🇸 United States

Dermapac, Inc.

DI: 10810102270075 · Model: 1815 · Dermapac Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

Basic Information

Brand Name
Dermapac, Inc.
Primary DI
10810102270075
Version / Model
1815
Company Name
Dermapac Inc.
Labeler DUNS
796088466
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
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
1802006d-c460-4b6d-b068-95741e6b8a85

Device Description

Fluffs 18"x18" 15 ply

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
44971 General-purpose surgical sponge

Identifiers

Type ID
Unit of Use 00810102270078
Primary 10810102270075

Customer Contacts

Phone
203-924-7148