FDA UDI Not in Commercial Distribution 🇺🇸 United States

MICTEC NERVE PROTECTOR

DI: B09920942120 · Model: 20942-12 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MICTEC NERVE PROTECTOR
Primary DI
B09920942120
Version / Model
20942-12
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-30
Public Version
6
Public Version Date
2023-12-19
Public Version Status
Update
Public Device Record Key
be29f322-7f16-4ab9-91b6-b6832102ce58
Distribution End Date
2018-09-28

Device Description

MICTEC NERVE PROTECTOR CURVED LEFT ANGLED DOWN

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
No
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", "Dry Heat Sterilization"]

Product Codes

Code Name
GCJ Laparoscope, General & Plastic Surgery

GMDN Terms

Code Name
46768 Nerve/vessel retractor

Identifiers

Type ID
Primary B09920942120

Customer Contacts

Phone
800-821-7496

Premarket Submissions

Submission Number Supplement Number
K002877 000

Device Sizes

Type Value Unit Text
Length 300 Millimeter