FDA UDI Not in Commercial Distribution 🇺🇸 United States

V. Mueller

DI: 10885403185083 · Model: NL9702-1 · CAREFUSION 2200, INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
V. Mueller
Primary DI
10885403185083
Version / Model
NL9702-1
Catalog Number
NL9702-1
Company Name
CAREFUSION 2200, INC
Labeler DUNS
832696038
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
3
Public Version Date
2019-12-11
Public Version Status
Update
Public Device Record Key
9370a690-b820-4283-b926-1d1220adab0c
Distribution End Date
2019-01-23

Device Description

MCCULLOCH RETRACTOR BLADE SET INCLUDES 1 SET NL9702-110, NL9702-120 NL9702-230, NL9702-240

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
Yes
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
GZT RETRACTOR, SELF-RETAINING, FOR NEUROSURGERY

GMDN Terms

Code Name
45181 Surgical retraction system, reusable

Identifiers

Type ID
Primary 10885403185083

Customer Contacts