FDA UDI In Commercial Distribution 🇺🇸 United States

Gossen Metrawatt SECULIFE

DI: 00863313000347 · Model: DF+ · BC GROUP INTERNATIONAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Gossen Metrawatt SECULIFE
Primary DI
00863313000347
Version / Model
DF+
Catalog Number
M695P
Company Name
BC GROUP INTERNATIONAL, INC.
Labeler DUNS
602930208
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
d2cdfb8b-3266-4501-8a6a-3b919bdb38ed

Device Description

Defibrillator Analyzer, with Transcutaneous Pacemaker Input - private labeled for Gossen Metrawatt

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DRL Tester, Defibrillator

GMDN Terms

Code Name
36791 External defibrillator tester

Identifiers

Type ID
Primary 00863313000347

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K110192 000