FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046963319625 · Model: SW474T · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04046963319625
Version / Model
SW474T
Catalog Number
SW474T
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-22
Public Version
3
Public Version Date
2020-07-30
Public Version Status
Update
Public Device Record Key
332e1b06-6318-498c-8434-cdb31c6959db

Device Description

S4 MONOAXIAL SCREW 8.5X40MM CANULATED

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
NKB Orthosis, spinal pedicle fixation, for degenerative disc disease

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 04046963319625

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Length : 40.000 MM
Device Size Text, specify Diameter (mm) : 8.500 MM