FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00885556569351 · Model: 7207705D · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00885556569351
Version / Model
7207705D
Catalog Number
7207705D
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-15
Public Version
3
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
181d9418-d25d-4275-a8be-210bf40b2a6e

Device Description

RFBDRIVER3.5MM2.0MM CANN W/HUD ADAP

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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
32865 Orthopaedic implant driver

Identifiers

Type ID
Primary 00885556569351

Customer Contacts