FDA UDI In Commercial Distribution 🇺🇸 United States

PLASMAFIT

DI: 04046964093395 · Model: NT403R · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
PLASMAFIT
Primary DI
04046964093395
Version / Model
NT403R
Catalog Number
NT403R
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-08
Public Version
2
Public Version Date
2021-11-15
Public Version Status
Update
Public Device Record Key
89f77a97-158a-4e74-8164-678006f03511

Device Description

PLASMAFIT TRAY F/MODULE SCREW FIXATION

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
FSM TRAY, SURGICAL, INSTRUMENT

GMDN Terms

Code Name
42997 Surgical instrument/implant rack

Identifiers

Type ID
Primary 04046964093395

Customer Contacts