FDA UDI In Commercial Distribution 🇺🇸 United States

Integra® Padgett® Dermatomes

DI: 10381780277965 · Model: 3539252 · INTEGRA LIFESCIENCES CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
Integra® Padgett® Dermatomes
Primary DI
10381780277965
Version / Model
3539252
Catalog Number
3539252
Company Name
INTEGRA LIFESCIENCES CORPORATION
Labeler DUNS
963856096
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2018-10-17
Public Version
2
Public Version Date
2021-06-22
Public Version Status
Update
Public Device Record Key
c1fe618c-3ba1-4529-afc1-f6dfd904d5eb

Device Description

Blade, Dermatome (For Models S, SB, B and C)(6 languages)

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
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
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GFD DERMATOME

GMDN Terms

Code Name
35134 Dermatome blade, single-use

Identifiers

Type ID
Secondary M24835392521
Primary 10381780277965
Unit of Use 00381780277968

Customer Contacts