Identity
- Trade Name
- RESORB X FDA UDI
- Generic Name
- Surgical water bath system FDA UDI
- Device Name
- XCELSIOR WATER BATH, COVER FDA UDI
- Model / Reference
- 52-400-13-04 FDA UDI
- Description
- XCELSIOR WATER BATH, COVER FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00888118084798 FDA UDI
- FDA Product Code
- IRQ FDA UDI
- GMDN Term
- Surgical water bath system FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5950 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
Moist Heat or Steam Sterilization FDA UDI
Category: Surgical water bath system
Resorb X by KLS-Martin L.P. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Surgical water bath system.
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- RESORB X — KLS-Martin L.P. · Class I
- RESORB X — KLS-Martin L.P. · 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 |
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Manufacturer
- Manufacturer
- KLS-Martin L.P.
Sources (1)
- FDA UDI 79b617b3-7f10-410e-b409-5054e7f2da4b 34 fields · synced May 31, 2026