FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 04055207011683 · Model: 898811 · Richard Wolf GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
NA
Primary DI
04055207011683
Version / Model
898811
Catalog Number
8988.11
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
2024-11-21
Public Version Status
Update
Public Device Record Key
27a9d186-3bc4-43d7-b9ab-073c4a1154b9
Distribution End Date
2018-06-30

Device Description

OBTURATOR FOR HYSTEROSCOPE 21FR for WL 205mm, distal tip dull, compatible with sheath 898803 21Fr for diagnostic hysteroscopy, 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
Yes
PM Exempt
Yes
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, Hydrogen Peroxide, Ethylene Oxide

Product Codes

Code Name
FEC OBTURATOR, FOR ENDOSCOPE

GMDN Terms

Code Name
35692 Rigid endoscope obturator

Identifiers

Type ID
Primary 04055207011683

Customer Contacts

Phone
+497043350

Device Sizes

Type Value Unit Text
Outer Diameter 7 Millimeter