FDA UDI In Commercial Distribution 🇺🇸 United States

Single Use Needle Guide

DI: 05704916000882 · Model: UA1339 · Bk Medical ApS
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Single Use Needle Guide
Primary DI
05704916000882
Version / Model
UA1339
Company Name
Bk Medical ApS
Labeler DUNS
310093901
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-09
Public Version
10
Public Version Date
2024-02-16
Public Version Status
Update
Public Device Record Key
06da4b99-3291-4b6a-8690-fd18a046b91d

Device Description

Sterile-packed. Bore diameter 1.6 mm; angle of insertion 0° to the long axis of the transducer

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FCG Biopsy Needle

GMDN Terms

Code Name
45018 Needle guide, single-use

Identifiers

Type ID
Package 05704916000899
Primary 05704916000882

Customer Contacts

Phone
+4544528100