FDA UDI Not in Commercial Distribution 🇺🇸 United States

Instrument

DI: 05060296233693 · Model: imcirpr · Stanmore Implants Worldwide Ltd
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Instrument
Primary DI
05060296233693
Version / Model
imcirpr
Catalog Number
IMCIRPR
Company Name
Stanmore Implants Worldwide Ltd
Labeler DUNS
494989502
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-07-18
Public Version
2
Public Version Date
2023-06-05
Public Version Status
Update
Public Device Record Key
c45b3146-58dd-4242-af08-ee86f2e1282b
Distribution End Date
2023-06-02

Device Description

Circlip Pliers

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
No
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
KRO Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer

GMDN Terms

Code Name
44795 Manual orthopaedic bender, reusable

Identifiers

Type ID
Primary 05060296233693

Premarket Submissions

Submission Number Supplement Number
K092138 000
K133152 000