FDA UDI In Commercial Distribution 🇺🇸 United States

KIT KE063 COLE

DI: 20607915129358 · Model: GK208 · APPLIED MEDICAL RESOURCES CORPORATION
Product Codes
5
GMDN Terms
4
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KIT KE063 COLE
Primary DI
20607915129358
Version / Model
GK208
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
cf55c8e8-d561-4d6d-9f39-b6592c18bb4c

Device Description

Kit Contains: CTB12, 5x100 Kii SH BLD ZTHR DP 10/BX CTB33, 11X100 Kii SH BLD ZTHR 6/BX C6001, 5mmX33cm PROB/VALV DUAL BAG 12/BX CA090, DIRECT DRIVE LCA 3/BX C2201, 120MM INSUFF NEEDLE XE, 20/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)
FHF System, Evacuator, Fluid
GCJ Laparoscope, General & Plastic Surgery
MDM Instrument, Manual, Surgical, General Use
FZP Clip, Implantable

GMDN Terms

Code Name
12750 Spring-loaded pneumoperitoneum needle, single-use
47342 Laparoscopic irrigation/aspiration cannula
42412 Laparoscopic access cannula, single-use
35649 Ligation clip, metallic

Identifiers

Type ID
Primary 20607915129358

Customer Contacts