FDA UDI Not in Commercial Distribution 🇺🇸 United States

STERIFLEX HT

DI: M695RAHT010090 · Model: RAHT-01009 · Tyber Medical, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
STERIFLEX HT
Primary DI
M695RAHT010090
Version / Model
RAHT-01009
Catalog Number
RAHT-01009
Company Name
Tyber Medical, LLC
Labeler DUNS
010968002
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-12-19
Public Version
4
Public Version Date
2025-08-15
Public Version Status
Update
Public Device Record Key
10bba463-a340-4759-b369-3da230fc598c
Distribution End Date
2024-07-25

Device Description

Mini Fixed AO Handle w/ Ø0.9mm Guidewire (6") Kit

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
44052 Orthopaedic surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Primary M695RAHT010090

Customer Contacts