FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046963147037 · Model: PO800SU · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
6

Basic Information

Brand Name
AESCULAP
Primary DI
04046963147037
Version / Model
PO800SU
Catalog Number
PO800SU
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
6
Record Status
Published
Publish Date
2016-09-23
Public Version
7
Public Version Date
2020-07-01
Public Version Status
Update
Public Device Record Key
24d4efe1-982f-4fd8-b332-f89234f39a5c

Device Description

DISP.COMBINATION INSTR.BIPOLAR D:5/310MM

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
Primary 04046963147037
Unit of Use 04038653457564

Customer Contacts