FDA UDI In Commercial Distribution 🇺🇸 United States

SPATIAL FRAME

DI: 00885556012871 · Model: 71070365 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SPATIAL FRAME
Primary DI
00885556012871
Version / Model
71070365
Catalog Number
71070365
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-25
Public Version
5
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
66a13d24-c47c-409c-8bb1-b8e59f44faa5

Device Description

SPATIAL FRAME ROCKER RING

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
MR Unsafe
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
IPR CRUTCH

GMDN Terms

Code Name
48011 External orthopaedic fixation system, single-use

Identifiers

Type ID
Primary 00885556012871

Customer Contacts