Microsafe

MICROSAFE, 10 ul short

Registry build 21.09.26
16manufacturers in China registered for this device type
24catalogue numbers in this listing
4recalls on this code

Who Else Makes It

Concentrated in Jiangsu (4), Shandong (4), Zhejiang (3). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code GIO
Manufacturer City Province Registered as Device types
Hangzhou Rollmed Co., Ltd. Hangzhou Zhejiang Contract manufacturer 127
Weihai Kangzheng Medical Equipments Technology Co., Ltd. Weihai Shandong Contract manufacturer 26
Boen Healthcare Co., Ltd. Suzhou Jiangsu Specification developer 263
Infitek Co., Ltd. Shanghai Shanghai Manufacturer 49
Diatrust Medical Co., Ltd. Nanjing Jiangsu Manufacturer 48
Labpeak Co., Ltd. Jinan Shandong Manufacturer 43
Scitek Global Co., Ltd. Jinan Shandong Manufacturer 43
Zhejiang Gongdong Medical Technology Co., Ltd. Taizhou Zhejiang Contract manufacturer 40
Weihai Kangzhou Biotechnology Engineering Co., Ltd. Weihai Shandong Manufacturer 24
Xiamen Zhiyuan Medical Technology Co., Ltd. Xiamen Fujian Contract manufacturer 22
Zhejiang Saining Biotechnology Co., Ltd. Taizhou Zhejiang Manufacturer 12
Medico Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 11

Showing 12 of 16. All 16 manufacturers in China registered for Tube, Collection, Capillary Blood

Record

Regulatory record for Microsafe
Listed by Drummond Scientific Co., United States
FDA product code GIO
Device type Tube, Collection, Capillary Blood
Device class Class 1
Regulation 21 CFR 864.6150
Establishment Manufacturer
Premarket notification Exempt
Record published 2025-02-05
Record revised 2025-03-14 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for Microsafe
Catalogue number Size Per pack Status
1010-50-D 50 In distribution
1005 2,000 In distribution
1020-50-D 50 In distribution
1080 2,000 In distribution
1030-50-D 50 In distribution
1050 2,000 In distribution
1010S 2,000 In distribution
1015 2,000 In distribution
1050-100 100 In distribution
1015-50-D 50 In distribution
1035 2,000 In distribution
1025-50-D 50 In distribution
1025 2,000 In distribution
1017 2,000 In distribution
1075 2,000 In distribution
1035-25-01 25 In distribution
1050-50-D 50 In distribution
1060 2,000 In distribution
1040 2,000 In distribution
1030 2,000 In distribution
1010 2,000 In distribution
1020 2,000 In distribution
1015-10-D 10 In distribution
1040-25 25 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Globe Scientific Globe Scientific, LLC 25
LT Tube for PRP Zhuhai Longtime Biological Technology Co., Ltd. 13
LT Kit for PRP Zhuhai Longtime Biological Technology Co., Ltd. 12
Baixin Anhui Kangda Medical Products Co., Ltd. 10
QBC Diagnostics Drucker Diagnostics, LLC 8
Microsafe® Safe-Tec Clinical Products, Inc. 8
MultiCap pH/ Blood Gas/Na+/K+/Ca++/Cl-/Glu/Lac/tHb Siemens Healthcare Diagnostics Inc 7
Safe-T-Fill® Ram Scientific 7
McKesson Mckesson Medical-Surgical Inc. 6
pts collect™ Capillary Tubes Polymer Technology Systems 6
MultiCap-S pH/ Blood Gas/Na+/K+/Ca++/Cl-/Glu/Lac/tHb Siemens Healthcare Diagnostics Inc 6
Marketlab Inc Marketlab Incorporated 4

Showing 12 of 120. All products under Tube, Collection, Capillary Blood

Recalls

The FDA has not published a severity grade for these. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2008-08-01 Not classified Material/Component Contamination presence of OSCS contaminant 1000 vials 2008-12-18
2008-08-01 Not classified Material/Component Contamination presence of OSCS contaminant 4000 vials 2008-12-18
2008-08-01 Not classified Material/Component Contamination presence of OSCS contaminant 2000 vials 2008-12-18
2008-08-01 Not classified Material/Component Contamination presence of OSCS contaminant 12,000 vials 2008-12-18

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer