Identity
- Trade Name
- BR Surgical, LLC FDA UDI
- Generic Name
- Surgical/emergency suction cannula, non-illuminating, single-use FDA UDI
- Device Name
- TEARDROP Controlled Suction Tube, single-use, Gray, Ø 10FR, WL 4”, OL 6 1/4”, 10/box FDA UDI
- Model / Reference
- BR99-29247 FDA UDI
- Description
- TEARDROP Controlled Suction Tube, single-use, Gray, Ø 10FR, WL 4”, OL 6 1/4”, 10/box FDA UDI
Identifiers
- Catalog Number
- BR99-29247 FDA UDI
- Primary DI / UDI-DI
- 00840183524883 FDA UDI
- FDA Product Code
- GEA FDA UDIJOL FDA UDIJZF FDA UDI
- GMDN Term
- Surgical/emergency suction cannula, non-illuminating, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI880.6740 FDA UDI874.4420 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
Single Use
Yes
Implantable
No
Contains Latex
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
Yes
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
Yes
Manufacturing Date
Yes
Category: Surgical/emergency suction cannula, non-illuminating, single-use
The BR Surgical, LLC TEARDROP Controlled Suction Tube is a single-use, gray medical device designed for controlled suction use in various surgical and emergency procedures. It features a rigid/semi-rigid design with an atraumatic tip, providing precise aspiration of body cavities, wounds, or surgical sites. This tube is not dedicated to dental, intrauterine, or liposuction procedures.
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Authorization Coverage (1 country)
Regulatory Authorizations
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Br Surgical Llc
Sources (1)
- FDA UDI c9a47a6a-293d-4b55-be72-ce6a84e64346 35 fields · synced Jul 24, 2026