FDA UDI In Commercial Distribution 🇺🇸 United States

Dermapac, Inc.

DI: 10810102270952 · Model: 7104 · Dermapac Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

Basic Information

Brand Name
Dermapac, Inc.
Primary DI
10810102270952
Version / Model
7104
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
f7df5119-94e4-40d9-8bd4-2cf73f360b81

Device Description

#32 Latex Free Rubber Bands 2/pk

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
KDC Instrument, Surgical, Disposable

GMDN Terms

Code Name
33961 General surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Unit of Use 00810102270955
Primary 10810102270952

Customer Contacts

Phone
203-924-7148