FDA UDI In Commercial Distribution 🇺🇸 United States

Activa Instrument

DI: E302BIS65059 · Model: B-IS-6505 · Bioretec Oy
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Activa Instrument
Primary DI
E302BIS65059
Version / Model
B-IS-6505
Catalog Number
B-IS-6505
Company Name
Bioretec Oy
Labeler DUNS
368715301
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-20
Public Version
4
Public Version Date
2020-04-06
Public Version Status
Update
Public Device Record Key
1f220c46-7daf-44a0-8c93-b57c2b0ff8d2

Device Description

Protection sheath

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
35095 Surgical drill guide, reusable

Identifiers

Type ID
Primary E302BIS65059

Customer Contacts