FDA UDI In Commercial Distribution 🇺🇸 United States

Biover

DI: 07640174510368 · Model: MI8039 · Biover AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Biover
Primary DI
07640174510368
Version / Model
MI8039
Catalog Number
MI8039
Company Name
Biover AG
Labeler DUNS
482102712
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-02-28
Public Version
2
Public Version Date
2023-04-18
Public Version Status
Update
Public Device Record Key
a0bce7f5-5bf6-4a41-8a69-3c09b4f69ae0

Device Description

Titanium micro forceps for vascular surgery, platform, 180mm length, 0.2mm tip, 8mm grip

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
DWS Instruments, Surgical, Cardiovascular

GMDN Terms

Code Name
12726 Suturing needle holder, reusable

Identifiers

Type ID
Primary 07640174510368

Customer Contacts

Phone
+41416300022

Device Sizes

Type Value Unit Text
Outer Diameter 0.2 Millimeter
Length 180 Millimeter