Globe Scientific

Capillary Tube, Microhematocrit, Soda Lime Glass, Green Tip, Ammonium Heparinized, 100/Vial, 10 Vials/Unit

Registry build 21.09.26
16manufacturers in China registered for this device type
25catalogue numbers in this listing

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 Globe Scientific
Listed by Globe Scientific, LLC, United States
FDA product code GIO
Device type Tube, Collection, Capillary Blood
Device class Class 1
Regulation 21 CFR 864.6150
Establishment Repacker / relabeller, Complaint-file establishment
Premarket notification Exempt
Record published 2019-11-26
Record revised 2021-02-19 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Label carries lot or batch number, expiry date
Packaging Case of 10

Catalogue Numbers

Catalogue numbers for Globe Scientific
Catalogue number Size Per pack Status
51688 1,000 In distribution
51680 1,000 In distribution
52162 1,000 In distribution
165313 1,000 In distribution
51684 1,000 In distribution
172513 300 In distribution
165413 1,000 In distribution
172292 1,000 In distribution
51608 1,000 In distribution
182313 1,000 In distribution
165513 1,000 In distribution
173313 1,000 In distribution
51635 1,000 In distribution
155113 1,000 In distribution
172213 1,000 In distribution
167313 1,000 In distribution
174313 1,000 In distribution
51613 1,000 In distribution
51686 1,000 In distribution
117713 1,000 In distribution
174113 1,000 In distribution
124413 1,000 In distribution
164113 1,000 In distribution
51628 1,000 In distribution
51602 1,000 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Microsafe Drummond Scientific Co. 24
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 Naming This Product

1 recall names this product by its own identifier, the UDI on its label.

Recalls naming the identifiers of Globe Scientific
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Medica Corp. UDI-DI 2025-12-31 Class II Nonconforming Material/Component A systematic positive bias of up to 20% was identified across the reportable potassium range, resulting in false elevation results of patient samples when using Medica s capillary tubes. 1,578 units

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