Identity
- Trade Name
- Test Bag, 50mL FDA UDI
- Generic Name
- Respiratory oxygen therapy system FDA UDI
- Model / Reference
- 60298 FDA UDI
Identifiers
- Catalog Number
- 60298 FDA UDI
- Primary DI / UDI-DI
- 04942962602983 FDA UDI
- FDA Product Code
- BTL FDA UDI
- GMDN Term
- Respiratory oxygen therapy system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5925 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
Yes
FDA UDI
Prescription Use
No
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Total Volume — 50 Milliliter FDA UDI
Category: Respiratory oxygen therapy system
Test Bag, 50mL by Atom Medical Corp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Respiratory oxygen therapy system.
- 02-RESQ — Pulmodyne Inc. · Class II
- 02-RESQ — Pulmodyne Inc. · Class II
- GO-PAP — Pulmodyne Inc. · Class II
- O2-RESQ — Pulmodyne Inc. · Class II
- HI-OXYGEN MASK ADULT W/O VALVE, WITH 7FT TUBE, SINGLE PACKING — BESMED HEALTH BUSINESS CORP. · Class I
- O2-MAX — Pulmodyne Inc. · Class II
- Infant Flow™ — VYAIRE MEDICAL, INC. · Class II
- AincA — Anesthesia Associates, 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
- Atom Medical Corp
Sources (1)
- FDA UDI dc0f2f5e-c918-43a4-bdb0-9e660d354d99 35 fields · synced May 29, 2026