FDA UDI In Commercial Distribution 🇺🇸 United States

CESPACE

DI: 04038653351497 · Model: FJ102R · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CESPACE
Primary DI
04038653351497
Version / Model
FJ102R
Catalog Number
FJ102R
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
2
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
a9df61a8-34c0-4587-a126-12cada9a1f66

Device Description

CESPACE BONE IMPACTOR

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
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
HWA IMPACTOR

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 04038653351497

Customer Contacts