FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10886982269713 · Model: 60.133.000 · Synthes GmbH
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
NA
Primary DI
10886982269713
Version / Model
60.133.000
Catalog Number
60133000
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-05
Public Version
5
Public Version Date
2026-04-17
Public Version Status
Update
Public Device Record Key
74f0a7b7-663f-472b-b7db-a36ea3928b60

Device Description

OUTER CASE LID 3/3 WIDTH/ ALUM

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
No
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
FSM TRAY, SURGICAL, INSTRUMENT
KCT Sterilization wrap containers, trays, cassettes & other accessories

GMDN Terms

Code Name
42997 Surgical instrument/implant rack

Identifiers

Type ID
Direct Marking 07612334122438
Primary 10886982269713

Customer Contacts