FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046963343446 · Model: PO893SU · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

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Basic Information

Brand Name
AESCULAP
Primary DI
04046963343446
Version / Model
PO893SU
Catalog Number
PO893SU
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-09-24
Public Version
10
Public Version Date
2024-08-07
Public Version Status
Update
Public Device Record Key
e4231514-8a56-46a5-9b0a-004dfc0f4785

Device Description

ADTEC SINGLE USE Grasping Forceps, shaft only, (310 mm), diam. 5 mm, fenestrated, double action, sterile, reposable, to be used with: PM950R, PM951R, PM953R, PM954R, PM957R, PO958R, PO959R, package of 10 pieces

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
58039 Endoscopic electrosurgical handpiece/electrode, monopolar, single-use

Identifiers

Type ID
Primary 04046963343446
Unit of Use 04046963183080

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Diameter (mm) : 5.000 MM
Device Size Text, specify Working length (mm) : 310.000 MM