FDA UDI In Commercial Distribution 🇺🇸 United States

Stealth

DI: 00811714035871 · Model: 918001-0000-P · RESPONSIVE ORTHOPEDICS LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Stealth
Primary DI
00811714035871
Version / Model
918001-0000-P
Catalog Number
918001-0000-P
Company Name
RESPONSIVE ORTHOPEDICS LLC
Labeler DUNS
002745858
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-16
Public Version
1
Public Version Date
2023-10-24
Public Version Status
New
Public Device Record Key
87688eb6-57df-41d6-9358-32e633e7580e

Device Description

Stealth Instruments

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
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
FSM Tray, Surgical, Instrument

GMDN Terms

Code Name
12143 Instrument tray, reusable

Identifiers

Type ID
Primary 00811714035871