FDA UDI In Commercial Distribution 🇺🇸 United States

Integra® Padgett® Dermatomes

DI: 10381780282341 · Model: 3539250230 · INTEGRA LIFESCIENCES CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Integra® Padgett® Dermatomes
Primary DI
10381780282341
Version / Model
3539250230
Catalog Number
3539250230
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
b495fb92-8831-4007-b8cd-f65ec905e32e

Device Description

Model B (230V) - Dermatome Complete Kit

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Has Manufacturing Date
Yes
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 M24835392502301
Primary 10381780282341

Customer Contacts