Identity
- Trade Name
- EMI Super Micro Scissors FDA UDI
- Generic Name
- Vascular scissors FDA UDI
- Device Name
- Operate the handle of this product to cut the suture during surgery. The blade tip opens and closes due to the repulsive action of the spring. It refers to an instrument used for cutting sutures during surgery. It consists of two blades with a rotating axis and is operated by closing the two blades on the material to be cut. FDA UDI
- Model / Reference
- EMI092D FDA UDI
- Description
- Operate the handle of this product to cut the suture during surgery. The blade tip opens and closes due to the repulsive action of the spring. It refers to an instrument used for cutting sutures during surgery. It consists of two blades with a rotating axis and is operated by closing the two blades on the material to be cut. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04582486866920 FDA UDI
- FDA Product Code
- HNF FDA UDI
- GMDN Term
- Vascular scissors FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4350 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
No
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Vascular scissors
EMI Super Micro Scissors by Emi Factory Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Vascular scissors.
- PILLING — TELEFLEX INCORPORATED · Class I
- Novo Surgical — NOVO SURGICAL, INC. · Class I
- Ambler Surgical — Ambler Surgical, LLC · Class I
- Sklar® — Sklar Corporation · Class I
- Adler Instrument Company — Adler, Inc. · Class I
- PILLING — TELEFLEX INCORPORATED · Class I
- PILLING — TELEFLEX INCORPORATED · Class I
- BOSS Instruments — Boss Instruments, Ltd. · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Emi Factory Co., Ltd.
Sources (1)
- FDA UDI 517172c7-62a3-415d-be5f-1af3fe9db6af 34 fields · synced Jun 8, 2026