FDA UDI In Commercial Distribution 🇺🇸 United States

FERGUSON TENACULUM FORCEPS

DI: 00192896044579 · Model: 508-532 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
FERGUSON TENACULUM FORCEPS
Primary DI
00192896044579
Version / Model
508-532
Catalog Number
508-532
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-14
Public Version
3
Public Version Date
2019-08-21
Public Version Status
Update
Public Device Record Key
f01735f9-9107-4657-b100-e5a0dc18397d

Device Description

FERGUSON TENACULUM CLAMP FORCEPS STRAIGHT JAW

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
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
GEN FORCEPS, GENERAL & PLASTIC SURGERY

GMDN Terms

Code Name
62468 Surgical soft-tissue manipulation forceps, scissors-like, reusable

Identifiers

Type ID
Primary 00192896044579

Customer Contacts

Device Sizes

Type Value Unit Text
Length 6.75 Inch