Medical Consumable Disposable 10ml Oral Syringe Baby Feeding Syringe
Overview
Essential details
- Place of Origin:
-
Anhui, China
- Brand Name:
-
TKMD
- Model Number:
-
None
- Disinfecting Type:
-
EO sterilization
- Properties:
-
Dental Equipments & Accessories, Medical Polymer Materials & Products
- Size:
-
11cm
- Stock:
-
NO
- Shelf Life:
-
3 years
- Material:
-
PP
- Quality Certification:
-
ce
- Instrument classification:
-
Class III
- Safety standard:
-
ISO 7886
- Package:
-
PE or blister
- MOQ:
-
100000
- Port:
-
Shanghai
- Keyword:
-
10ml oral syringe
- Certificate:
-
CE ISO13485
- Payment Term:
-
T/T or others
- OEM:
-
Accept OEM
- Capacity:
-
10-20 Hundred Thousand Pcs/month
Supply Ability
- Supply Ability
- 10000 Piece/Pieces per Week
Packaging & delivery
- Packaging Details
Small Package:PE/Blister
Medium Package:Medium box/Medium PE bag
Outer Package:Carton
- Port
shanghai
- Picture Example:
-
- Lead time:
-
Quantity(pieces) 1 – 100000 100001 – 1000000 >1000000 Lead time (days) 30 35 To be negotiated
Product Description
Related model
Certifications
Company Profile
Anhui Tiankang Medical Technology Co.,Ltd (Stock Abbreviation: Tiankang Medical, Stock Code: 835942) have got official new three board on March 3, 2016 and now we have a registered capital of 57.78 million RMB yuan. We specialize in developing and producing products like safety syringes with retractable needles, auto disable syringes, I.V sets ,T.V sets ,extracorporeal blood circuits for haemodialysers,oral syringes, I.V catheter and intravenous infusion sets with burette etc.
What deserves to be mentioned the most is that we are authorized European CE certificate (in 2002),ISO13485 certificate (in 2002) and WHO—PQS certificate (in 2010) which we hold as passports to enter international market. Our company’s products began to be registered with the U.S. Food and Drug Administration in 2012 and currently rank among the best in the country for U.S. Food and Drug Administration-listed products. Autonomic products: safety syringes with retractable needles which registered by U.S. Food and Drug Administration 510K, disposable syringes and disposable hypodermic needles also passed U.S. Food and Drug Administration registered 510K. From June 6 ,2016 to June 9, with zero defect through the U.S. Food and Drug Administration field QSR 820 audit at the U.S. Food and Drug Administration site.
National government leaders visiting
Factory view
Shippment
Exhibition
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