FDA UDI Not in Commercial Distribution 🇺🇸 United States

V. Mueller

DI: 10885403067945 · Model: 007-01 · STERIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
V. Mueller
Primary DI
10885403067945
Version / Model
007-01
Catalog Number
00701
Company Name
STERIS CORPORATION
Labeler DUNS
021599373
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-21
Public Version
8
Public Version Date
2025-11-24
Public Version Status
Update
Public Device Record Key
e93714f1-3456-43dc-9f0b-9845a41950cc
Distribution End Date
2024-11-06

Device Description

V. Mueller VERRES NEEDLE 150MM DISPOSABLE 12/BX

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
FHO pneumoperitoneum needle

GMDN Terms

Code Name
12750 Spring-loaded pneumoperitoneum needle, single-use

Identifiers

Type ID
Package 20885403067942
Primary 10885403067945

Customer Contacts