FDA UDI In Commercial Distribution 🇺🇸 United States

WEITLANER/HENLEY RETRACTOR CENTER BLADE

DI: 00192896092808 · Model: 230-512 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
WEITLANER/HENLEY RETRACTOR CENTER BLADE
Primary DI
00192896092808
Version / Model
230-512
Catalog Number
230-512
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-03
Public Version
2
Public Version Date
2022-11-01
Public Version Status
Update
Public Device Record Key
7f602907-278f-452c-8725-be29dac63003

Device Description

WEITLANER/HENLEY RETRACTOR CENTER BLADE

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
GAD Retractor

GMDN Terms

Code Name
45182 Self-retaining surgical retractor, reusable

Identifiers

Type ID
Primary 00192896092808

Customer Contacts

Device Sizes

Type Value Unit Text
Length 3.5 Inch