Identity
- Trade Name
- Valvulotome 23cm, blade 2mm, w/ball FDA UDI
- Generic Name
- Valvulotome FDA UDI
- Device Name
- Valvulotome 23cm, blade 2mm, w/ball FDA UDI
- Model / Reference
- 03-7510 FDA UDI
- Description
- Valvulotome 23cm, blade 2mm, w/ball FDA UDI
Identifiers
- Catalog Number
- 03-7510 FDA UDI
- Primary DI / UDI-DI
- 04057034015322 FDA UDI
- FDA Product Code
- MGZ FDA UDI
- GMDN Term
- Valvulotome FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.4885 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Valvulotome
Valvulotome 23cm, blade 2mm, w/ball by Geister Medizin Technik GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Valvulotome.
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- PILLING — TELEFLEX INCORPORATED · Class I
- PILLING — TELEFLEX INCORPORATED · Class I
- Antegrade and Retrograde LeMills Valvulotome — LeMaitre Vascular, Inc. · Class II
- Over-the-Wire LeMaitre Valvulotome — LeMaitre Vascular, Inc. · Class II
- V. Mueller — STERIS CORPORATION · Class I
- Symmetry Surgical — SYMMETRY SURGICAL INC. · Class II
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 |
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Manufacturer
- Manufacturer
- Geister Medizin Technik GmbH
Sources (1)
- FDA UDI 553eba26-a915-4dea-8c47-af47aa0eeb7a 35 fields · synced May 30, 2026