FDA UDI In Commercial Distribution 🇺🇸 United States

Padgett Replacement Dermatome Blades Sterile

DI: 90850010779280 · Model: 9.1999 · Robbins Instruments Inc
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
Padgett Replacement Dermatome Blades Sterile
Primary DI
90850010779280
Version / Model
9.1999
Catalog Number
9.1999
Company Name
Robbins Instruments Inc
Labeler DUNS
002182269
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2019-10-25
Public Version
3
Public Version Date
2021-06-22
Public Version Status
Update
Public Device Record Key
b6699a34-c2f9-4ed4-acdc-ce33dd039ad5

Device Description

Padgett Replacement Dermatome Blades Sterile 100mm

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
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
GFA BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL

GMDN Terms

Code Name
35134 Dermatome blade, single-use

Identifiers

Type ID
Primary 90850010779280
Unit of Use 10850010779284

Customer Contacts