FDA UDI In Commercial Distribution 🇺🇸 United States

STANDARD KIT 4

DI: 20607915129136 · Model: GK201 · APPLIED MEDICAL RESOURCES CORPORATION
Product Codes
4
GMDN Terms
4
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
STANDARD KIT 4
Primary DI
20607915129136
Version / Model
GK201
Company Name
APPLIED MEDICAL RESOURCES CORPORATION
Labeler DUNS
187129135
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-09
Public Version
4
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
fde2fea2-de9c-4805-86f0-4c9ac900c5d1

Device Description

Kit Contains: CTR12, 5x100 Kii OPT ZTHR DP 10/BX CTB33, 11X100 Kii SH BLD ZTHR 6/BX CTS12, 11x100 Kii SLEEVE ZTHR 12/BX C2201, 120MM INSUFF NEEDLE XE, 20/BX CD001, 10mm RETRIEVAL SYSTEM, 10/BX CA090, DIRECT DRIVE LCA 3/BX

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
HET Laparoscope, Gynecologic (And Accessories)
GCJ Laparoscope, General & Plastic Surgery
FZP Clip, Implantable
MDM Instrument, Manual, Surgical, General Use

GMDN Terms

Code Name
45130 Tissue extraction bag
12750 Spring-loaded pneumoperitoneum needle, single-use
42412 Laparoscopic access cannula, single-use
35649 Ligation clip, metallic

Identifiers

Type ID
Primary 20607915129136

Customer Contacts