Identity
- Trade Name
- VESSEL CLAMP, BLUE FDA UDI
- Generic Name
- Surgical A/V-shaped microvessel clamp FDA UDI
- Device Name
- A hand-held surgical instrument designed to compress the severed end of a small vessel (e.g., blood vessel, vas deferens) to occlude the vessel, typically prior to anastomosis formation. Often referred to as an Acland clamp, it has an A-/V-shaped design whereby the vessel is slid into the mouth of the clamp up to the apex where it is compressed; it does not have a hinge/jaws (i.e., it is not forceps or a bulldog clamp). This is a reusable device intended to be sterilized prior to use. FDA UDI
- Model / Reference
- 201003NS FDA UDI
- Description
- A hand-held surgical instrument designed to compress the severed end of a small vessel (e.g., blood vessel, vas deferens) to occlude the vessel, typically prior to anastomosis formation. Often referred to as an Acland clamp, it has an A-/V-shaped design whereby the vessel is slid into the mouth of the clamp up to the apex where it is compressed; it does not have a hinge/jaws (i.e., it is not forceps or a bulldog clamp). This is a reusable device intended to be sterilized prior to use. FDA UDI
Identifiers
- Catalog Number
- 201003NS FDA UDI
- Primary DI / UDI-DI
- B066201003NS1 FDA UDI
- 510(k) Number
- K801395 FDA UDI
- FDA Product Code
- DXC FDA UDI
- GMDN Term
- Surgical A/V-shaped microvessel clamp FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.4450 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Ethylene Oxide FDA UDI
Category: Surgical A/V-shaped microvessel clamp
Vessel Clamp, Blue by Novosci Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical A/V-shaped microvessel clamp.
- LAZIC — Peter Lazic GmbH · Class I
- Novo Surgical — NOVO SURGICAL, INC. · Class II
- Novo Surgical — NOVO SURGICAL, INC. · Class II
- Novo Surgical — NOVO SURGICAL, INC. · Class II
- Novo Surgical — NOVO SURGICAL, INC. · Class II
- Novo Surgical — NOVO SURGICAL, INC. · Class II
- Novo Surgical — NOVO SURGICAL, INC. · Class II
- LAZIC — Peter Lazic GmbH · Class I
Cleared under the same submission
K801395 also covers:
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
- Novosci Corp.
Sources (1)
- FDA UDI 985715eb-dbf3-4e8a-8cca-e671fc7e1070 36 fields · synced May 30, 2026