FDA UDI In Commercial Distribution 🇺🇸 United States

Dermapac, Inc.

DI: 10810102270136 · Model: 2080-B · Dermapac Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

Basic Information

Brand Name
Dermapac, Inc.
Primary DI
10810102270136
Version / Model
2080-B
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
dd089b6c-137f-4058-a854-0fe8b350c3f4

Device Description

Sponge Pack (5 pack 8"x4" gauze) wrapped

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 00810102270139
Primary 10810102270136

Customer Contacts

Phone
203-924-7148