iQIBLA's Zikr Ring Flex Lite is a Smarter, Sleeker and Lighter Tasbih Ring for Muslim prayers, The Zikr Ring is designed to meet the needs of Muslims for tasbih and prayer times reminder, replacing the traditional Muslims prayer beads with a smart and neat wearable technology ring. The ring provides many functions, including a Smart Tasbih Counter upto 9999, reminder of the Two to five time daily prayers, 3 Tasbih Time Reminder With OLED Display, Comes With 3 Compatible Sizes(18mm / 20mm / 22mm)
SPECIFICATIONS:
Ring Size : 3 Compatible Sizes(18mm / 20mm / 22mm)
Product Weight : 7.7gm
Packing Size(cm) : 7.6*7.6*4.0
Packing Weight : 166gm
Material : Polymer
Bluetooth : Bluetooth 5.1
Supporting OS : Android 5.1 or iOS 10.0 or Later
Screen : OLED, 0.42inch, 62*40mm
Battery : 50mAh
Button : 1 Button
Charging Port : Pogo Pin - UAB C Type
Theoretical Working Hours : upto 7 days in typical usage / upto days in basic usage
Sensors : Vibration Motor
Size Available : 22mm, 20mm, 18mm
PACKAGING INCLUDES:
1* Smart Zikr ring with 3 Sizes attachments
Zikr1 Lite Ring, iQIBLA's world's first smart ring for Muslim prayers: "The Zikr1 Lite Ring is designed to meet the needs of Muslims for tasbih and prayer times reminding, replacing the traditional Muslims prayer beads with a smart and neat wearable technology ring. The ring provides many functions, including a reminder of the five daily prayers, a Tasbih counter, in addition to displaying the time."
Zikr1 Lite Ring is the world's first Muslim smart ring, Applying the trendy wearable technology to serve the Muslim.
SPECIFICATIONS
Product Weight : 7.7gm
Packing Size(cm) : 7.5*7.4*4.2
Packing Weight : 50gm
Material : Plastic
Bluetooth : Bluetooth 5.1
Supporting OS : Android 5.1 or iOS 10.0 or Later
Screen : OLED, 0.49inch, 72*40
Battery : 40mAh
Button : 1 Button
Charging Port : Jack Port
Theoretical Working Hours : upto 3 days in typical usage/upto 5 days in basic usage
Sensors : Vibration Motor
Size Available : 22mm,20mm,18mm
Pacing Includes : 1*Zikr1 Lite Ring, 1* USB Cable, 1* User Manual
Ppe items, mask, face shield, isolation gowns, gloves, and covid test kits, toys, electronics, cell phones, hardware, pp raw material or polypropylene.
Indication: Qualitative detection of nucleic acid from SARS-CoV-2 in upper
and lower respiratory specimens (such as anterior nasal swabs, mid-turbinate nasal swabs, nasopharyngeal swabs, oropharyngeal swabs, sputum, lower respiratory tract aspirates, bronchoalveolar lavage, and nasopharyngeal wash/aspirate or nasal aspirate) from individuals suspected of COVID-19 by their healthcare provider.
Emergency use of this test is limited to authorized laboratories.
Authorized Laboratories: Laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. 263a, to perform high
complexity tests.
This letter is in response to your1 request that the Food and Drug Administration (FDA) issue an Emergency Use Authorization (EUA) for emergency use of your product,2 pursuant to Section 564 of the Federal Food, Drug, and Cosmetic Act (the Act) (21 U.S.C. 360bbb-3). On February 4, 2020, pursuant to Section 564(b)(1)(C) of the Act, the Secretary of the
Department of Health and Human Services (HHS) determined that there is a public health emergency that has a significant potential to affect national security or the health and security of United States citizens living abroad, and that involves the virus that causes COVID-19.
Pursuant to Section 564 of the Act, and on the basis of such determination, the Secretary of HHS then declared that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of the virus that causes COVID-19 subject to the terms of any authorization issued under Section 564(a) of the Act.
Having concluded that the criteria for issuance of this authorization under Section 564(c) of the Act are met, I am authorizing the emergency use of your product, described in the Scope of Authorization of this letter (Section II), subject to the terms of this authorization.
I. Criteria for Issuance of Authorization I have concluded that the emergency use of your product meets the criteria for issuance of an authorization under Section 564(c) of the Act, because I have concluded that:
1. The SARS-CoV-2 can cause a serious or life-threatening disease or condition,
including severe respiratory illness, to humans infected by this virus;
2. Based on the totality of scientific evidence available to FDA, it is reasonable to believe that your product may be effective in diagnosing COVID-19, and that the known and potential benefits of your product when used for diagnosing COVID-19, outweigh the known and potential risks of your product; and, 3. There is no adequate, approved, and available alternative to the emergency use of your
product.
4
II. Scope of Authorization
I have concluded, pursuant to Section 564(d)(1) of the Act, that the scope of this authorization is limited to the indication above.
Railway Track Trolley
Light Track Trolley/0.5T-1T loading capacity hand push trolley
For transporting material, equipment and tools on rail tracks.
Light, robust transport trolley with a platform of perforated aluminium plate with an anti-slip surface.
No accumulation of water or dirt.
Ball bearing synthetic running wheels/optionally sheet steel jacketed.
2 or 4 carrying handles in different positions.
Parking brake acting on two wheels.
Foldable type, easy to carry.
Various track gauges and designs on request.
