FDA UDI In Commercial Distribution 🇺🇸 United States

TC-PLUS Revision / RT-PLUS

DI: 07611996117714 · Model: 75100382 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TC-PLUS Revision / RT-PLUS
Primary DI
07611996117714
Version / Model
75100382
Catalog Number
75100382
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-11-25
Public Version
4
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
497a0f63-8f1d-40c6-a08b-574fb5baca04

Device Description

TC REVISION/RT/RT MODULAR EXTRACTION FORCEPS

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
Moist Heat or Steam Sterilization

Product Codes

Code Name
HTD FORCEPS

GMDN Terms

Code Name
42894 Implant handling forceps, scissors-like

Identifiers

Type ID
Primary 07611996117714

Customer Contacts