FDA UDI In Commercial Distribution 🇺🇸 United States

NEIVERT HOOK RETRACTOR

DI: 00192896098237 · Model: 199-408 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NEIVERT HOOK RETRACTOR
Primary DI
00192896098237
Version / Model
199-408
Catalog Number
199-408
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-07-11
Public Version
2
Public Version Date
2020-09-22
Public Version Status
Update
Public Device Record Key
11b30936-2f35-4f05-9fdd-013f58fb415a

Device Description

NEIVERT HOOK RETRACTOR

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 00192896098237

Customer Contacts

Phone
800-821-7496

Device Sizes

Type Value Unit Text
Length 8 Inch