FDA UDI Not in Commercial Distribution 🇺🇸 United States

INLINE

DI: 00885556724750 · Model: OM-9817 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
INLINE
Primary DI
00885556724750
Version / Model
OM-9817
Catalog Number
OM-9817
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-07-11
Public Version
3
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
6ba0b1a9-fb33-4e17-924e-15bd3447ac31
Distribution End Date
2022-03-17

Device Description

INLINE REUSABLE OBTURATOR SPEEDLOCK

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
No

Product Codes

Code Name
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
33997 Surgical drill guide obturator

Identifiers

Type ID
Primary 00885556724750

Customer Contacts