FDA UDI In Commercial Distribution 🇺🇸 United States

Integra® Padgett® Dermatomes

DI: 10381780277996 · Model: 3539800 · INTEGRA LIFESCIENCES CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Integra® Padgett® Dermatomes
Primary DI
10381780277996
Version / Model
3539800
Catalog Number
3539800
Company Name
INTEGRA LIFESCIENCES CORPORATION
Labeler DUNS
963856096
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-03-09
Public Version
2
Public Version Date
2021-06-22
Public Version Status
Update
Public Device Record Key
3a97a163-4597-4730-9997-49711b8f08df

Device Description

Model SB Slimline Dermatome Complete Unit - USA/Canada Only

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
GFD DERMATOME

GMDN Terms

Code Name
11179 Dermatome handpiece, electrically-powered

Identifiers

Type ID
Secondary M24835398001
Primary 10381780277996

Customer Contacts