FDA UDI In Commercial Distribution 🇺🇸 United States

Dornier MedTech

DI: 00810116021680 · Model: Bipolar Medium Bladder Loop 24 Fr Electrode-Sterile, Single-Use. (6/box) · DORNIER MEDTECH AMERICA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Dornier MedTech
Primary DI
00810116021680
Version / Model
Bipolar Medium Bladder Loop 24 Fr Electrode-Sterile, Single-Use. (6/box)
Catalog Number
BIPMBLA
Company Name
DORNIER MEDTECH AMERICA, INC.
Labeler DUNS
130789944
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-19
Public Version
1
Public Version Date
2020-06-29
Public Version Status
New
Public Device Record Key
e1e21294-dad7-44ce-9c17-7ff96ce04b83

Device Description

Bipolar Medium Bladder Loop 24 Fr Electrode-Sterile, Single-Use. (6/box)

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
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KNF Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)

GMDN Terms

Code Name
61872 Endoscopic electrosurgical electrode, bipolar, single-use

Identifiers

Type ID
Package 00810116021758
Primary 00810116021680