FDA UDI In Commercial Distribution 🇺🇸 United States

XEROFORM PETROLATUM

DI: 10381780471349 · Model: 77034 · Derma Sciences Canada Inc
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
XEROFORM PETROLATUM
Primary DI
10381780471349
Version / Model
77034
Catalog Number
DKC77034
Company Name
Derma Sciences Canada Inc
Labeler DUNS
200564891
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-13
Public Version
3
Public Version Date
2023-02-03
Public Version Status
Update
Public Device Record Key
6ec7e646-6408-41a4-9bb8-ef8c344fde6e

Device Description

Xeroform Petrolatum Impregnated Gauze

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GER GAUZE, EXTERNAL (WITH DRUG/BIOLOGIC/ANIMAL SOURCE MATERIAL)

GMDN Terms

Code Name
48132 Petrolatum woven gauze pad

Identifiers

Type ID
Package 30381780471343
Primary 10381780471349

Customer Contacts

Device Sizes

Type Value Unit Text
Width 1 Inch
Length 8 Inch
Width 2.5 Centimeter
Length 20.3 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Do not use if package is damaged