Identity
- Trade Name
- MICROVAC® FDA UDI
- Generic Name
- Surgical irrigation/aspiration handpiece, single-use FDA UDI
- Device Name
- ULTRA MALLEABLE SURGICAL SUCTION FDA UDI
- Model / Reference
- 3101-13 FDA UDI
- Description
- ULTRA MALLEABLE SURGICAL SUCTION FDA UDI
Identifiers
- Catalog Number
- 3101-13 FDA UDI
- Primary DI / UDI-DI
- 00650551038016 FDA UDI
- FDA Product Code
- JOL FDA UDI
- GMDN Term
- Surgical irrigation/aspiration handpiece, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Catheter Gauge — 13 French FDA UDI
Category: Surgical irrigation/aspiration handpiece, single-use
Microvac® by Pmt Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Medline — MEDLINE INDUSTRIES, INC. · Class II
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- Gyrus ACMI — Gyrus Acmi, Inc. · Class I
- GYRUS ACMI — Gyrus Acmi, 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 |
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Manufacturer
- Manufacturer
- Pmt Corp.
Sources (1)
- FDA UDI 85603900-780b-4932-95e8-467e3fdf55f0 37 fields · synced May 30, 2026