FDA UDI In Commercial Distribution 🇺🇸 United States

Skintact

DI: 19005531591520 · Model: RO21 /5 · Leonhard Lang GmbH
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
5

Basic Information

Brand Name
Skintact
Primary DI
19005531591520
Version / Model
RO21 /5
Catalog Number
RO21 /5
Company Name
Leonhard Lang GmbH
Labeler DUNS
302846407
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2016-06-01
Public Version
3
Public Version Date
2020-06-05
Public Version Status
Update
Public Device Record Key
d912b0bb-049e-4b67-8e5f-811f56d4e91c

Device Description

Neutral Electrode

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
58494 Electrosurgical return electrode, single-use

Identifiers

Type ID
Package 29005531591527
Primary 19005531591520
Unit of Use 09005531591523
Package 39005531591524

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 30 Degrees Celsius