FDA UDI Not in Commercial Distribution 🇺🇸 United States

CRANIOPLATE

DI: 04038653463909 · Model: FM963T · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CRANIOPLATE
Primary DI
04038653463909
Version / Model
FM963T
Catalog Number
FM963T
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-30
Public Version
5
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
9b994232-2d44-4b8b-8501-6a74337ae6e7
Distribution End Date
2021-10-25

Device Description

CRANIOPLATE 1.5 4HOLES STR.L:20MM

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
JEY PLATE, BONE

GMDN Terms

Code Name
61689 Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary 04038653463909

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Height : 0.600 MM