FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046955205288 · Model: PL774SU · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
6

Basic Information

Brand Name
AESCULAP
Primary DI
04046955205288
Version / Model
PL774SU
Catalog Number
PL774SU
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
6
Record Status
Published
Publish Date
2020-02-15
Public Version
2
Public Version Date
2021-10-25
Public Version Status
Update
Public Device Record Key
1b79ad02-829c-42a3-b4b2-33bdaca4e4d4

Device Description

CAIMAN MARYLAND NON ARTICULAT.D5/125MM

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, cutting & coagulation & accessories

GMDN Terms

Code Name
57944 Endoscopic electrosurgical handpiece/electrode, bipolar, single-use

Identifiers

Type ID
Unit of Use 04046955205271
Primary 04046955205288

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Working length (mm) : 125.000 MM
Device Size Text, specify Diameter (mm) : 5.000 MM