FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 04055207069837 · Model: 892408922 · 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
04055207069837
Version / Model
892408922
Catalog Number
892408922
Company Name
Richard Wolf GmbH
Labeler DUNS
315304071
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-01-14
Public Version
1
Public Version Date
2026-01-22
Public Version Status
New
Public Device Record Key
0c041fe0-1d6f-438e-84bf-55073e5960be

Device Description

KERRISON SHEATH W 2MM WL 130MM 90° for use with Kerrison handle, 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
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

Product Codes

Code Name
NBH Accessories, arthroscopic

GMDN Terms

Code Name
46688 Bone cutting forceps, reusable

Identifiers

Type ID
Primary 04055207069837

Customer Contacts

Phone
+497043350

Device Sizes

Type Value Unit Text
Length 130.0 Millimeter
Width 2.0 Millimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-20 – 60 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
10 – 90 Percent (%) Relative Humidity