FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 03596010468482 · Model: 7209485 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
NA
Primary DI
03596010468482
Version / Model
7209485
Catalog Number
7209485
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-11-13
Public Version
6
Public Version Date
2024-10-28
Public Version Status
Update
Public Device Record Key
d72de3d5-6814-4a99-a657-34541ee7ee5e

Device Description

MENISCUS MENDER II DISPOSABLE SET

Device Characteristics

Single Use
Yes
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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HWQ PASSER

GMDN Terms

Code Name
61143 Suturing needle, single-use

Identifiers

Type ID
Primary 03596010468482

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K885311 000