FDA UDI Not in Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04056702000493 · Model: PG082 · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
AESCULAP
Primary DI
04056702000493
Version / Model
PG082
Catalog Number
PG082
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-04-20
Public Version
6
Public Version Date
2022-02-25
Public Version Status
Update
Public Device Record Key
0e8fb060-970e-4527-a2f4-e600b56f8362
Distribution End Date
2021-08-02

Device Description

INSUFFLATION TUBE W/GAS PREHEATING

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
Yes
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
HIF INSUFFLATOR, LAPAROSCOPIC

GMDN Terms

Code Name
16779 Suction/irrigation tubing, single-use

Identifiers

Type ID
Primary 04056702000493

Customer Contacts