FDA UDI Not in Commercial Distribution 🇺🇸 United States

Skintact

DI: 19005531506494 · Model: DF82I · Leonhard Lang GmbH
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Skintact
Primary DI
19005531506494
Version / Model
DF82I
Catalog Number
DF82I
Company Name
Leonhard Lang GmbH
Labeler DUNS
302846407
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-06-16
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
9a7fc153-40d7-46b1-a695-245652147cfc
Distribution End Date
2015-06-17

Device Description

Multifunction electrode for defibrillation, pacing, cardioversion, and monitoring

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
Yes
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
MKJ Automated External Defibrillators (Non-Wearable)

GMDN Terms

Code Name
45806 Multifunction cardiac electrode, adult

Identifiers

Type ID
Package 39005531506498
Package 29005531506491
Primary 19005531506494

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 50 Degrees Celsius