FDA UDI Not in Commercial Distribution 🇺🇸 United States

JMA Optic Schütz

DI: B915011700200 · Model: 01170020 · zebris MEDICAL GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
JMA Optic Schütz
Primary DI
B915011700200
Version / Model
01170020
Catalog Number
NA
Company Name
zebris MEDICAL GmbH
Labeler DUNS
328971791
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-19
Public Version
2
Public Version Date
2021-02-19
Public Version Status
Update
Public Device Record Key
9df35221-1fac-4fda-b357-8496b88473c2
Distribution End Date
2021-02-17

Device Description

Opto-Electronik Face-Bow for monitoring and tracking of lower jaw movements

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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
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
NFS Device, Jaw Tracking, For Monitoring Jaw Positions

GMDN Terms

Code Name
35700 Facebow

Identifiers

Type ID
Primary B915011700200

Customer Contacts

Phone
+49600381444

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-20 – 70 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
0 – 95 Percent (%) Relative Humidity