FDA UDI Not in Commercial Distribution 🇺🇸 United States

QUINTEX

DI: 04046963814458 · Model: SC545T · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
QUINTEX
Primary DI
04046963814458
Version / Model
SC545T
Catalog Number
SC545T
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
8
Public Version Date
2025-11-20
Public Version Status
Update
Public Device Record Key
783c5ca7-9245-4b57-b8e2-a8757e2e37a1
Distribution End Date
2020-01-01

Device Description

QUINTEX HYBRID PLATE 4-LEVEL 79MM

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
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
KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

GMDN Terms

Code Name
46653 Spinal fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary 04046963814458

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Height : 2.000 MM