FDA UDI In Commercial Distribution 🇺🇸 United States

MAXFRAME

DI: 10886982261106 · Model: 03.312.001 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
MAXFRAME
Primary DI
10886982261106
Version / Model
03.312.001
Catalog Number
03312001
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-04-19
Public Version
3
Public Version Date
2022-05-02
Public Version Status
Update
Public Device Record Key
c02d07f5-7884-4b5c-8fef-79c4df0ed8b2

Device Description

WIRE TENSIONER

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
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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
32886 Wire holding/twisting forceps

Identifiers

Type ID
Direct Marking 07612334107237
Secondary H679033120010
Primary 10886982261106

Customer Contacts