FDA UDI In Commercial Distribution 🇺🇸 United States

N.A.

DI: EFOR22040811 · Model: -220-4081 · Forestadent Bernhard Förster GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

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Basic Information

Brand Name
N.A.
Primary DI
EFOR22040811
Version / Model
-220-4081
Company Name
Forestadent Bernhard Förster GmbH
Labeler DUNS
316074384
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2019-09-24
Public Version
1
Public Version Date
2019-10-02
Public Version Status
New
Public Device Record Key
1292dd5e-e0b0-420c-9204-9e5381e25c7b

Device Description

Betaflex Titan .032" for pendulum spring

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DZC WIRE, ORTHODONTIC

GMDN Terms

Code Name
16204 Orthodontic wire

Identifiers

Type ID
Primary EFOR22040811
Unit of Use EFOR220408111

Customer Contacts

Phone
+4972314590