ID Adapter

GUDID 27290108240904

Intradermal Adapter

WEST PHARMA. SERVICES IL, . LTD

Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use

• Primary Device ID: 27290108240904
• NIH Device Record Key: ec4be519-0042-4722-b364-b88b24aa49a5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ID Adapter
• Version Model Number: 5070204
• Company DUNS: 600267793
• Company Name: WEST PHARMA. SERVICES IL, . LTD
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290108240900 [Primary]
GS1	27290108240904 [Package]; Contains: 07290108240900; Package: [320 Units]; In Commercial Distribution

FDA Product Code

• FMF: Syringe, Piston

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: true

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

[27290108240904]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2019-10-07
• Device Publish Date: 2016-11-18

Devices Manufactured by WEST PHARMA. SERVICES IL, . LTD

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• 07290108241099 - Vial Adapter 20mm with silicon: 2023-06-23
• 07290108241105 - VA 13mm with Silicon: 2023-06-23
• 07290108241211 - Vial Adapter 13mm: 2023-06-23
• 17290108241331 - Vented Vial Adapter Transfer Device: 2022-12-01 Vented Vial Adapter 20mm FLL- VF
• 27290108240904 - ID Adapter: 2019-10-07Intradermal Adapter
• 27290108240904 - ID Adapter: 2019-10-07 Intradermal Adapter
• 27290108240577 - MP Vial Adapter 13 mm: 2019-07-22 MP Vial Adapter 13mm FLL – VF 3 Pack
• 27290108240683 - MP Vial Adapter 13 mm: 2019-07-22 MP Vial Adapter 13mm FLL – VF 5 Pack