Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Vascular dilator, reusable FDA UDI
- Device Name
- GARRETT VASC DILATOR TIP SZ 1MM 5-1/2IN FDA UDI
- Model / Reference
- CH5590-001 FDA UDI
- Description
- GARRETT VASC DILATOR TIP SZ 1MM 5-1/2IN FDA UDI
Identifiers
- Catalog Number
- CH5590001 FDA UDI
- Primary DI / UDI-DI
- 10885403027970 FDA UDI
- FDA Product Code
- DWP FDA UDI
- GMDN Term
- Vascular dilator, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.4475 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: Vascular dilator, reusable
V. Mueller by Steris Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Vascular dilator, reusable.
- Marina Medical — MARINA MEDICAL INSTRUMENTS, INC. · Class I
- Novo Surgical — NOVO SURGICAL, INC. · Class II
- Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
- RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
- Millennium — AVALIGN TECHNOLOGIES, Inc. · Class II
- Marina Medical — MARINA MEDICAL INSTRUMENTS, INC. · Class I
- HNM MEDICAL — HNM STAINLESS, LLC. · Class I
- Marina Medical — MARINA MEDICAL INSTRUMENTS, 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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Steris Corporation
Sources (1)
- FDA UDI 541a4151-908c-4aaa-bad5-80c26a05200b 35 fields · synced Jun 8, 2026