FDA UDI Not in Commercial Distribution 🇺🇸 United States

V. Mueller

DI: 10885403037870 · Model: F256.10030 · CAREFUSION 2200, INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
V. Mueller
Primary DI
10885403037870
Version / Model
F256.10030
Catalog Number
F256.10030
Company Name
CAREFUSION 2200, INC
Labeler DUNS
832696038
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
3
Public Version Date
2022-03-04
Public Version Status
Update
Public Device Record Key
2b59a45f-71bc-4faa-91d9-5c620cf8c58c
Distribution End Date
2020-08-24

Device Description

V. Mueller 10MM SPOON FORCEPS 32CM INSERT

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
GCJ Laparoscope, general & plastic surgery

GMDN Terms

Code Name
32684 Endoscopic electrosurgical handpiece/electrode, bipolar, reusable

Identifiers

Type ID
Primary 10885403037870

Customer Contacts