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BD Vacutainer® BD Vacutainer® blood collection tubes

BD バキュテイナ® EDTA 3K 入り採血管, コンベンショナル, 13 x 100, 7 mL

受注発注品

Overview

BD is the inventor of BD Vacutainer® blood collection tubes as well as the worldwide leader in blood tubes. We support our products with extensive clinical expertise and educational materials to help you achieve the best possible results.

true
Features and Benefits
Promotional Story
false
References
false
Specification

GTIN - each

00382903664504

1

GTIN - Case

50382903664509

1000

GTIN - Shelfpack

30382903664505

100


数量/箱

100本

数量/ケース

1000本


販売名

BD バキュテイナ採血管

承認/認証/届出番号

219AFBZX00109000

製造販売元

日本ベクトン・ディッキンソン株式会社


材質/素材

ガラス

チューブサイズ

外径13x長さ100 (mm)

採血量

7 mL

キャップタイプ / カラー

コンベンショナルキャップ/薄紫

ラベル

添加剤等

EDTA 3K

GTIN

GTIN - each 00382903664504 1
GTIN - Case 50382903664509 1000
GTIN - Shelfpack 30382903664505 100

梱包

数量/箱 100本
数量/ケース 1000本

薬事・その他情報

販売名 BD バキュテイナ採血管
承認/認証/届出番号 219AFBZX00109000
製造販売元 日本ベクトン・ディッキンソン株式会社

製品基本仕様

材質/素材 ガラス
チューブサイズ 外径13x長さ100 (mm)
採血量 7 mL
キャップタイプ / カラー コンベンショナルキャップ/薄紫
ラベル
添加剤等 EDTA 3K
References
false
Resources
References
false
Frequently Asked Questions
false
References
false
Related Products
RELATED PRODUCTS NOT AVAILABLE
References
false
Product Complaints
North American Regional Complaint Center
1-844-8BD-LIFE (1-844-823-5433)
Things to Consider

If you are a patient or end user, you can contact us yourself, or you may have your caregiver or your physician do that for you. To help us process your
information quickly and effectively, please contact our customer complaints
team.

To better facilitate our investigation, please include the following information in your reporting:


  • Product Name and/or Catalog Number
  • Lot Number or Serial Number
  • Any injuries and/or Harm?
  • What is the issue you experienced?
  • Is the actual sample or sample representative available? (If possible, please send affected sample)
  • Contact name and phone number
Product Recalls
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Recall Notifications
These recall notices provide current information on medical device recalls.
Learn more
References
false
false