FDA UDI In Commercial Distribution 🇺🇸 United States

Recon

DI: G3181016120 · Model: 10-1612 · Revelation Medical Devices
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Recon
Primary DI
G3181016120
Version / Model
10-1612
Catalog Number
10-1612
Company Name
Revelation Medical Devices
Labeler DUNS
122296421
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-12
Public Version
2
Public Version Date
2023-01-20
Public Version Status
Update
Public Device Record Key
9e648dda-cbc1-4955-832e-633545a7a004

Device Description

Wissinger Rod

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
No
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
MDM Instrument, Manual, Surgical, General Use

GMDN Terms

Code Name
35948 Endoscopic surgical probe

Identifiers

Type ID
Primary G3181016120

Customer Contacts

Phone
2609251382