FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04038653005024 · Model: GD125R · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04038653005024
Version / Model
GD125R
Catalog Number
GD125R
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-17
Public Version
2
Public Version Date
2022-09-19
Public Version Status
Update
Public Device Record Key
d45525c7-6408-416a-8fcc-55835df66bd0

Device Description

DIAMOND BURR D1.4MM/ISO 014 2.35X95MM

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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
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
HTT BURR, ORTHOPEDIC

GMDN Terms

Code Name
36249 Orthopaedic bur, reusable

Identifiers

Type ID
Primary 04038653005024

Customer Contacts