Identity
- Trade Name
- Medline FDA UDI
- Generic Name
- Oxygen quick-connect coupling, female FDA UDI
- Device Name
- DBD-PIPE NIPPLE,2.5" LONG,1/8" MNPT FDA UDI
- Model / Reference
- RTMPIPEM225 FDA UDI
- Description
- DBD-PIPE NIPPLE,2.5" LONG,1/8" MNPT FDA UDI
Identifiers
- Catalog Number
- RTMPIPEM225 FDA UDI
- Primary DI / UDI-DI
- 10193489025385 FDA UDI
- FDA Product Code
- BYX FDA UDI
- GMDN Term
- Oxygen quick-connect coupling, female FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5860 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
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Oxygen quick-connect coupling, female
Medline by Medline Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Oxygen quick-connect coupling, female.
- PC — Allied Medical LLC · Class I
- PC — Allied Medical LLC · Class I
- PC — Allied Medical LLC · Class I
- KENTEX — KENTRON HEALTH CARE, INC. · Class I
- PC — Allied Medical LLC · Class I
- HA, O2, INTL (DISSF X DISSF)15FT — Parker Hannifin Corp. · Class I
- PC — Allied Medical LLC · Class I
- PC — Allied Medical 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
- Medline Industries, Inc.
Sources (1)
- FDA UDI 8bdc9847-2d84-47f9-a52b-6d7c70b06cdf 35 fields · synced May 30, 2026