FDA UDI In Commercial Distribution 🇺🇸 United States

HI-LINE XS

DI: 04038653398546 · Model: GE522SU · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HI-LINE XS
Primary DI
04038653398546
Version / Model
GE522SU
Catalog Number
GE522SU
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-07
Public Version
3
Public Version Date
2020-07-23
Public Version Status
Update
Public Device Record Key
cdff9e47-82f0-4950-8ea3-2410cbf3d0b9

Device Description

HI-LINE XS DISP.LINDEMANN CUTTER II 12MM

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
Yes
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
GEY MOTOR, SURGICAL INSTRUMENT, AC-POWERED

GMDN Terms

Code Name
45553 Orthopaedic bur, single-use

Identifiers

Type ID
Primary 04038653398546

Customer Contacts