FDA UDI In Commercial Distribution 🇺🇸 United States

Activa Instrument

DI: 06438394001558 · Model: B-IS-9000 · 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
06438394001558
Version / Model
B-IS-9000
Catalog Number
B-IS-9000
Company Name
Bioretec Oy
Labeler DUNS
368715301
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-01-30
Public Version
1
Public Version Date
2026-02-09
Public Version Status
New
Public Device Record Key
7fd32914-54a0-43af-be67-cfdd4a99bc96

Device Description

Sterilization tray, for ActivaScrew™ instruments

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
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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
42997 Surgical instrument/implant rack

Identifiers

Type ID
Primary 06438394001558
Previous E302BIS90009

Customer Contacts