FDA UDI Not in Commercial Distribution 🇺🇸 United States

N/A

DI: 03596010471369 · Model: 7204670M · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
03596010471369
Version / Model
7204670M
Catalog Number
7204670M
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-12
Public Version
4
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
b1e73f0f-a097-4b0f-9601-61afb1ba113c
Distribution End Date
2022-03-17

Device Description

2ND GEN FORCEP POSTERIOR PUNCH

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
NBH ACCESSORIES,ARTHROSCOPIC

GMDN Terms

Code Name
35138 Meniscus knife

Identifiers

Type ID
Primary 03596010471369

Customer Contacts