FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 10705034716244 · Model: 03.616.025 · SYNTHES (U.S.A.) LP
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10705034716244
Version / Model
03.616.025
Catalog Number
03616025
Company Name
SYNTHES (U.S.A.) LP
Labeler DUNS
832637081
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-31
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
38025ec2-7a28-4261-a672-65d4fa295b04
Distribution End Date
2017-11-04

Device Description

HOLDING SLEEVE-LONG

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
47831 Orthopaedic implantation sleeve, reusable

Identifiers

Type ID
Direct Marking 07611819935761
Secondary H981036160250
Primary 10705034716244

Customer Contacts