FDA UDI In Commercial Distribution 🇺🇸 United States

MIASPAS

DI: 04038653265640 · Model: FK389R · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MIASPAS
Primary DI
04038653265640
Version / Model
FK389R
Catalog Number
FK389R
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-23
Public Version
1
Public Version Date
2020-05-01
Public Version Status
New
Public Device Record Key
e9fcbd0d-04f6-420d-a97a-7d260480936b

Device Description

MIASPAS TL RIB HEAD RESECTOR 120 DEG.

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
GEG ELEVATOR, SURGICAL, GENERAL & PLASTIC SURGERY

GMDN Terms

Code Name
31335 Bone curette, reusable

Identifiers

Type ID
Primary 04038653265640

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Length : 310.000 MM