Identity
- Trade Name
- CUSTOMED FDA UDI
- Generic Name
- Sputum specimen container IVD FDA UDI
- Device Name
- DISPOSABLE MUCUS TRAP, 80 ML (CC) FDA UDI
- Model / Reference
- 712057052781 FDA UDI
- Description
- DISPOSABLE MUCUS TRAP, 80 ML (CC) FDA UDI
Identifiers
- Catalog Number
- 9002781 FDA UDI
- Primary DI / UDI-DI
- M20890027810 FDA UDI
- FDA Product Code
- BYZ FDA UDI
- GMDN Term
- Sputum specimen container IVD FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Total Volume — 80 Milliliter FDA UDI
Category: Sputum specimen container IVD
Customed by Customed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Sputum specimen container IVD.
- Medichoice — OWENS & MINOR DISTRIBUTION, INC. · Class II
- ASP MEDICAL — Asp Global, LLC · Class II
- MediChoice — OWENS & MINOR DISTRIBUTION, INC. · Class II
- AMSure® Specimen Cup — AMSINO INTERNATIONAL, INC. · Class I
- AMSure® Specimen Container — AMSINO INTERNATIONAL, INC. · Class I
- Portex — ICU MEDICAL, INC. · Class I
- CUSTOMED — Customed, Inc. · Class II
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 II | Pending data |
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Manufacturer
- Manufacturer
- Customed, Inc.
Sources (1)
- FDA UDI 62d9bd9d-d5ad-4964-b0b7-498c1b093380 37 fields · synced Jun 8, 2026