FDA UDI In Commercial Distribution 🇺🇸 United States

Neivert Rhinoplastic Retractor

DI: 00192896104877 · Model: 199-398 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Neivert Rhinoplastic Retractor
Primary DI
00192896104877
Version / Model
199-398
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-21
Public Version
1
Public Version Date
2020-09-29
Public Version Status
New
Public Device Record Key
7cf11989-6ba9-47ae-9397-e359323f141d

Device Description

Neivert Rhinoplastic Retractor Double Ended Tips

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
Yes
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", "Dry Heat Sterilization"]

Product Codes

Code Name
GDG HOOK, SURGICAL, GENERAL & PLASTIC SURGERY

GMDN Terms

Code Name
42595 Soft-tissue surgical hook, reusable

Identifiers

Type ID
Primary 00192896104877

Customer Contacts

Device Sizes

Type Value Unit Text
Length 6.25 Inch