FDA UDI In Commercial Distribution 🇺🇸 United States

LUKENS THYMUS RETRACTOR

DI: 00192896092334 · Model: 502-410 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LUKENS THYMUS RETRACTOR
Primary DI
00192896092334
Version / Model
502-410
Catalog Number
502-410
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-04
Public Version
2
Public Version Date
2019-07-12
Public Version Status
Update
Public Device Record Key
9c4af8bf-9b80-44a2-bfda-c3522af2de0e

Device Description

LUKENS THYMUS RETRACTOR BLUE ELECTRO COATED

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
["Dry Heat Sterilization", "Moist Heat or Steam Sterilization"]

Product Codes

Code Name
KAL Retractor, Ent

GMDN Terms

Code Name
35047 ENT elevator

Identifiers

Type ID
Primary 00192896092334

Customer Contacts

Device Sizes

Type Value Unit Text
Length 7 Inch