FDA UDI In Commercial Distribution 🇺🇸 United States

PROBE

DI: B974P6180 · Model: PROBE · DR.FRIGZ INTERNATIONAL(PVT)LTD,
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
PROBE
Primary DI
B974P6180
Version / Model
PROBE
Catalog Number
P618
Company Name
DR.FRIGZ INTERNATIONAL(PVT)LTD,
Labeler DUNS
645680125
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-21
Public Version
1
Public Version Date
2022-11-29
Public Version Status
New
Public Device Record Key
e02650ac-fe1b-4949-bd55-282bf0208557

Device Description

PROBE 5"

Device Characteristics

Single Use
Yes
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
Ethylene Oxide

Product Codes

Code Name
KDC Instrument, Surgical, Disposable

GMDN Terms

Code Name
63722 Ophthalmic soft-tissue surgical forceps probe-tip, single-use

Identifiers

Type ID
Primary B974P6180

Device Sizes

Type Value Unit Text
Length 5 Inch