Identity
- Trade Name
- CATHETER FDA UDI
- Generic Name
- Eustachian catheter, reusable FDA UDI
- Device Name
- EAR, HARTMANN, NO. 2 FDA UDI
- Model / Reference
- 36-321-02-01 FDA UDI
- Description
- EAR, HARTMANN, NO. 2 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00888118057693 FDA UDI
- FDA Product Code
- GBY FDA UDI
- GMDN Term
- Eustachian catheter, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4200 FDA UDI
- Commercial Distribution
- Not 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
Moist Heat or Steam Sterilization FDA UDI
Catheter by KLS-Martin L.P. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- KLS-Martin L.P.
Sources (1)
- FDA UDI 00edf5c6-9b5f-4915-a6a0-26a0882a68fb 36 fields · synced Jun 1, 2026