Identity
- Trade Name
- Busse Hospital Disposables FDA UDI
- Generic Name
- Nasal aspirator, manual FDA UDI
- Device Name
- 2 oz. Ear/Ulcer Bulb Syringe, Red FDA UDI
- Model / Reference
- 140 FDA UDI
- Description
- 2 oz. Ear/Ulcer Bulb Syringe, Red FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00849233000063 FDA UDI
- FDA Product Code
- KYZ FDA UDI
- GMDN Term
- Nasal aspirator, manual FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6960 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
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Ethylene Oxide FDA UDI
Category: Nasal aspirator, manual
Busse Hospital Disposables by Robert Busse & Co., Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Nasal aspirator, manual.
- Dr. Brown's — Dr. Brown's Company · Class I
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class I
- Muc-Away, Comfort Soft — WESTMED, INC. · Class II
- Safety 1st — DOREL JUVENILE GROUP, INC. · Class I
- Muc-Away — WESTMED, INC. · Class II
- Braun — KAZ USA, INC. · Class I
- Safety 1st — DOREL JUVENILE GROUP, INC. · Class I
- DeRoyal — DEROYAL INDUSTRIES, INC. · 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
- Robert Busse & Co., Inc.
Sources (1)
- FDA UDI 59a9cebf-fd4b-429f-8133-1c6babc4c175 34 fields · synced May 31, 2026