Identity
- Trade Name
- VYGON FDA UDI
- Generic Name
- Phlebotomy kit FDA UDI
- Device Name
- BLOOD DRAW KIT W/CHLORAPREP FDA UDI
- Model / Reference
- AMS-729CP-1 FDA UDI
- Description
- BLOOD DRAW KIT W/CHLORAPREP FDA UDI
Identifiers
- Catalog Number
- AMS-729CP-1 FDA UDI
- Primary DI / UDI-DI
- 08498840002179 FDA UDI
- FDA Product Code
- CBT FDA UDI
- GMDN Term
- Phlebotomy kit FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.1100 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Phlebotomy kit
Vygon by Vygon Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Phlebotomy kit.
- Aero-Med — AERO-MED LLC · Class I
- CARDINAL HEALTH — Cardinal Health 200, LLC · N
- Aero-Med — AERO-MED LLC · Class I
- Medline — MEDLINE INDUSTRIES, INC. · Class II
- Aero-Med — AERO-MED LLC · Class I
- Aero-Med — AERO-MED LLC · Class I
- CARDINAL HEALTH — Cardinal Health 200, LLC · Class I
- Aero-Med — AERO-MED LLC · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Vygon Corp.
Sources (1)
- FDA UDI f1b6ba26-fa81-4373-8ddb-376acf8e05f1 34 fields · synced Jun 6, 2026