FDA UDI Not in Commercial Distribution 🇺🇸 United States

ENDO-CARTRIS

DI: 04055207021668 · Model: 8891121 · Richard Wolf GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ENDO-CARTRIS
Primary DI
04055207021668
Version / Model
8891121
Catalog Number
8891.121
Company Name
Richard Wolf GmbH
Labeler DUNS
315304071
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-28
Public Version
5
Public Version Date
2023-05-26
Public Version Status
Update
Public Device Record Key
ffe4ab6d-7edc-40a2-bc59-5adb67a263fc
Distribution End Date
2018-11-30

Device Description

OBTURATOR SZ 5MM for introduction sleeve 8891021, reusable

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["Moist Heat or Steam Sterilization", "Ethylene Oxide", "Hydrogen Peroxide"]

Product Codes

Code Name
HRX ARTHROSCOPE

GMDN Terms

Code Name
35692 Rigid endoscope obturator

Identifiers

Type ID
Primary 04055207021668

Customer Contacts

Phone
+497043350