FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046963130367 · Model: GC927R · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
AESCULAP
Primary DI
04046963130367
Version / Model
GC927R
Catalog Number
GC927R
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-07-29
Public Version
1
Public Version Date
2022-08-08
Public Version Status
New
Public Device Record Key
ddbcefef-e33d-4b2d-b384-4126953f9677

Device Description

SHANK F/GC615R/GC633R ON GB130R/GB391R

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HWE INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT

GMDN Terms

Code Name
44985 Surgical saw blade, reciprocating, reusable

Identifiers

Type ID
Primary 04046963130367

Customer Contacts