Primary Device ID | 10724995184701 |
NIH Device Record Key | 3738d55b-6146-4491-bf7c-d87953f96391 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 710201 |
Catalog Number | 710201 |
Company DUNS | 627879687 |
Company Name | US Endoscopy |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | true |
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 |
Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Device Issuing Agency | Device ID |
---|---|
GS1 | 00724995184704 [Primary] |
GS1 | 10724995184701 [Package] Contains: 00724995184704 Package: Case [50 Units] In Commercial Distribution |
KDQ | BOTTLE, COLLECTION, VACUUM |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-07-04 |
Device Publish Date | 2022-06-24 |
00724995244545 - Lumiflex | 2025-06-11 LUMIFLEX 3-STAGE Balloon Dilatation Catheter 5.5cm/6mm wire is made of nylon and is a progressive stage balloon capable of three |
00724995244552 - Lumiflex | 2025-06-11 LUMIFLEX 3-STAGE Balloon Dilatation Catheter 5.5cm/8mm wire is made of nylon and is a progressive stage balloon capable of three |
00724995244569 - Lumiflex | 2025-06-11 LUMIFLEX 3-STAGE Balloon Dilatation Catheter 5.5cm/10mm wire is made of nylon and is a progressive stage balloon capable of thre |
00724995244576 - Lumiflex | 2025-06-11 LUMIFLEX 3-STAGE Balloon Dilatation Catheter 5.5cm/12mm wire is made of nylon and is a progressive stage balloon capable of thre |
00724995244583 - Lumiflex | 2025-06-11 LUMIFLEX 3-STAGE Balloon Dilatation Catheter 5.5cm/15mm wire is made of nylon and is a progressive stage balloon capable of thre |
00724995244590 - Lumiflex | 2025-06-11 LUMIFLEX 3-STAGE Balloon Dilatation Catheter 5.5cm/18mm wire is made of nylon and is a progressive stage balloon capable of thre |
00724995244606 - Lumiflex | 2025-06-11 LUMIFLEX 3-STAGE Balloon Dilatation Catheter 5.5cm/6mm no wire is made of nylon and is a progressive stage balloon capable of th |
00724995244613 - Lumiflex | 2025-06-11 LUMIFLEX 3-STAGE Balloon Dilatation Catheter 5.5cm/8mm no wire is made of nylon and is a progressive stage balloon capable of th |