FDA UDI In Commercial Distribution 🇺🇸 United States

Blade for Dermatome 100mm

DI: ENOU19199 · Model: 1919 · Nouvag AG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Blade for Dermatome 100mm
Primary DI
ENOU19199
Version / Model
1919
Company Name
Nouvag AG
Labeler DUNS
480610476
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2018-08-21
Public Version
2
Public Version Date
2021-06-22
Public Version Status
Update
Public Device Record Key
bb0c0c67-8f8a-49e6-a815-2e2bcc55f9ae

Device Description

Blade for Dermatome 100mm

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
Primary ENOU19199
Unit of Use ENOU19190

Customer Contacts

Phone
+41718466600