FDA UDI In Commercial Distribution 🇺🇸 United States

LAZIC

DI: 04250603735342 · Model: 69.321.01 · Peter Lazic GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LAZIC
Primary DI
04250603735342
Version / Model
69.321.01
Catalog Number
69.321.01
Company Name
Peter Lazic GmbH
Labeler DUNS
327681359
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-01-22
Public Version
1
Public Version Date
2020-01-30
Public Version Status
New
Public Device Record Key
5a3be8d9-9d6e-4130-8501-4465519fae86

Device Description

Bipolar forceps, Non-Stick, Straight Tip 0,7 mm x 6 mm, with Crrigation, 160 mm length, US-Pin Connector

Device Characteristics

Single Use
No
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
47848 Open-surgery electrosurgical handpiece/electrode, bipolar, reusable

Identifiers

Type ID
Primary 04250603735342

Customer Contacts