FDA UDI In Commercial Distribution 🇺🇸 United States

Needle Guide

DI: 10841436123249 · Model: 810-401 · CIVCO MEDICAL INSTRUMENTS CO., INC.
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
Needle Guide
Primary DI
10841436123249
Version / Model
810-401
Catalog Number
810-401, 810-401-5
Company Name
CIVCO MEDICAL INSTRUMENTS CO., INC.
Labeler DUNS
134614411
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-06-20
Public Version
1
Public Version Date
2024-06-28
Public Version Status
New
Public Device Record Key
04c9c7c7-16b3-48b2-ac9f-9432139f6b25

Device Description

Sterile endocavity needle guide for use with International Biomedical E717 6.5 MHz, Mindray 65EB10EA, 6CV1, 6CV1s, EV6.5Mhz/R10, V10-4, V10-4s, V11-3s, V11-3Ws, Samsung Medison EC4-9ES, EC4-9IS, ER4-9ES, Siemens 6.5EC10, SuperSonic E12-3, SE12-3, SEV12-3 transducers One-cell MEA: =80% embryo developed to expand cytoblast at 96 hours USP Endotoxin (LAL) tested and passed with 20 EU or less per device.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
ITX Transducer, ultrasonic, diagnostic
MQE NEEDLE, ASSISTED REPRODUCTION

GMDN Terms

Code Name
45018 Needle guide, single-use

Identifiers

Type ID
Package 00841436123259
Primary 10841436123249
Package 00841436123242

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K231783 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep Away from Sunlight