PURblue

PURblue in bottle blister, 0.5-0.85mm granules, 5cc

Registry build 21.09.26
2manufacturers in China registered for this device type
22catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shanghai (1), Beijing (1).

Chinese manufacturers registered for FDA product code MQV
Manufacturer City Province Registered as Device types
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Allgens Medical Technology Co., Ltd. Beijing Beijing Complaint-file establishment 1

Record

Regulatory record for PURblue
Listed by Orthogem, Ltd., United Kingdom
FDA product code MQV
Device type Filler, Bone Void, Calcium Compound
Device class Class 2
Regulation 21 CFR 888.3045
510(k) K150064
Record published 2015-11-18
Record revised 2018-07-06 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Distribution end date 2016-07-31

Catalogue Numbers

Catalogue numbers for PURblue
Catalogue number Size Status
P1102-1205 In distribution
P1102-1210 In distribution
P1102-1412 In distribution
P1103-1210 In distribution
P1104-2405 In distribution
P1102-1208 In distribution
P3107-0002 In distribution
P1104-0805 In distribution
P1103-1215 In distribution
P1104-1205 In distribution
P1103-2415 In distribution
P1103-2420 In distribution
P1104-1202 In distribution
P1103-2410 In distribution
P1104-0802 In distribution
P1102-1405 In distribution
P1103-2430 In distribution
P3107-0001 In distribution
P1102-1408 In distribution
P1102-1212 In distribution
P1102-1410 In distribution
P3107-0003 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Synthacer medArtis Medizinprodukte und Forschung Aktiengesellschaft 360
Syntricer medArtis Medizinprodukte und Forschung Aktiengesellschaft 357
Biosorb S.B.M 65
MagnetOs Kuros Biosciences B.V 61
BioSet® Rti Surgical, Inc. 47
Bicera® Resorbable Bone Substitute Wiltrom Corporation Limited 41
GRAFTON®and Grafton PLUS®Demineralized Bone Matrix (DBM) Medtronic Sofamor Danek, Inc. 40
Bicera® Resorbable Bone Substitute Wiltrom Co., Ltd. (Chutung) 39
ChronOS Synthes Gmbh 39
Synthacer/Syntricer medArtis Medizinprodukte und Forschung Aktiengesellschaft 36
Inion BioRestore™ Inion OY 35
Resorba Synthetic Bone Biomatlante 35

Showing 12 of 750. All products under Filler, Bone Void, Calcium Compound

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K150064 2015-09-04
K110787 2011-04-21
K070132 2007-07-13

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