FDA UDI In Commercial Distribution 🇺🇸 United States

CRANIOPLATE

DI: 04046963173852 · Model: FM992T · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CRANIOPLATE
Primary DI
04046963173852
Version / Model
FM992T
Catalog Number
FM992T
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-30
Public Version
3
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
3608ccad-a1c7-4f6c-bd54-965837b4db16

Device Description

CRANIOPLATE 1.5 KIT 4MM CROS.BURR.COVER

Device Characteristics

Single Use
Yes
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
No
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
JEY PLATE, BONE

GMDN Terms

Code Name
61688 Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile

Identifiers

Type ID
Primary 04046963173852

Customer Contacts