FDA UDI In Commercial Distribution 🇺🇸 United States

HI-LINE

DI: 04038653070107 · Model: GB538R · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HI-LINE
Primary DI
04038653070107
Version / Model
GB538R
Catalog Number
GB538R
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-20
Public Version
1
Public Version Date
2020-04-28
Public Version Status
New
Public Device Record Key
60baae7b-06c1-4d62-866a-044a239d70c2

Device Description

HI-LINE FIXED DURAGUARD III

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
Yes
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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
GET MOTOR, SURGICAL INSTRUMENT, PNEUMATIC POWERED

GMDN Terms

Code Name
43555 Burring power tool attachment

Identifiers

Type ID
Primary 04038653070107

Customer Contacts