FDA UDI In Commercial Distribution 🇺🇸 United States

Activa Instrument

DI: 06438394009066 · Model: B-II-0815 · Bioretec Oy
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Activa Instrument
Primary DI
06438394009066
Version / Model
B-II-0815
Catalog Number
B-II-0815
Company Name
Bioretec Oy
Labeler DUNS
368715301
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-01-26
Public Version
1
Public Version Date
2026-02-03
Public Version Status
New
Public Device Record Key
39c4c436-0999-40fb-b9d8-e65c57c305ee

Device Description

K-wire Ø0.8mm, length 150 mm, for 4.0/5.0/6.0 mm interference screw

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
Yes
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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
46165 Orthopaedic guidewire, reusable

Identifiers

Type ID
Primary 06438394009066
Previous E302BII08159

Customer Contacts

Device Sizes

Type Value Unit Text
Length 150 Millimeter
Width 0.8 Millimeter