FDA UDI In Commercial Distribution 🇺🇸 United States

REDI-LOCK™

DI: 00190730087997 · Model: 501-002U-S · ORTHO TECHNOLOGY, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
REDI-LOCK™
Primary DI
00190730087997
Version / Model
501-002U-S
Company Name
ORTHO TECHNOLOGY, INC.
Labeler DUNS
781772017
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-09-16
Public Version
1
Public Version Date
2021-09-24
Public Version Status
New
Public Device Record Key
ad21addb-ef21-434e-ad65-1751f3d450dd

Device Description

REDI-LOCK™ IMPRESSION TRAYS PEDO MEDIUM UPPER-ORANGE 50PK

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
Yes
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
EHY TRAY, IMPRESSION, PREFORMED

GMDN Terms

Code Name
16350 Dental impression tray, single-use

Identifiers

Type ID
Primary 00190730087997