FDA UDI In Commercial Distribution 🇺🇸 United States

Dermapac, Inc.

DI: 10810102270549 · Model: 6003 · Dermapac Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

Basic Information

Brand Name
Dermapac, Inc.
Primary DI
10810102270549
Version / Model
6003
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
529a3703-f5c5-4682-a10f-4fe5e6924419

Device Description

Tonsil Sponges x ray detectable 1-1/4" 5/pack

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
38496 Radiopaque woven surgical sponge

Identifiers

Type ID
Unit of Use 00810102270542
Primary 10810102270549

Customer Contacts

Phone
203-924-7148