FDA UDI In Commercial Distribution 🇺🇸 United States

LiNA PowerBlade™

DI: 05708265018284 · Model: 5010-160 · LiNA Medical AG
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
LiNA PowerBlade™
Primary DI
05708265018284
Version / Model
5010-160
Company Name
LiNA Medical AG
Labeler DUNS
485705870
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-04-03
Public Version
1
Public Version Date
2026-04-13
Public Version Status
New
Public Device Record Key
0abd0ce4-19f0-4136-9afa-7584b5cde799

Device Description

Bipolar cutting & coagulation forceps, straight jaws, ø 10mm, 185 mm working length, 3 m cable, 2 x 4 mm pins.

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
57944 Endoscopic electrosurgical handpiece/electrode, bipolar, single-use

Identifiers

Type ID
Package 05708265018291
Primary 05708265018284
Package 05708265018307