Identity
- Trade Name
- Duval Forcep FDA UDI
- Generic Name
- Flexible endoscopic sponge/swab forceps FDA UDI
- Model / Reference
- MM-600-003S FDA UDI
Identifiers
- Catalog Number
- MM-600-003S FDA UDI
- Primary DI / UDI-DI
- G390MM600003S0 FDA UDI
- FDA Product Code
- HTD FDA UDI
- GMDN Term
- Flexible endoscopic sponge/swab forceps FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Flexible endoscopic sponge/swab forceps
Duval Forcep by Ntz Surgical Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Flexible endoscopic sponge/swab forceps.
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- V. Mueller — STERIS CORPORATION · Class I
- PRIMO/ASP MEDICAL — Asp Global, LLC · Class I
- PILLING — TELEFLEX INCORPORATED · Class I
- PILLING — TELEFLEX INCORPORATED · Class I
- Duval Forcep — NTZ SURGICAL COMPANY · Class I
- Duval Forcep — NTZ SURGICAL COMPANY · 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 |
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Manufacturer
- Manufacturer
- Ntz Surgical Company
Sources (1)
- FDA UDI c7b10420-3647-4592-a7a8-21c2ef085f66 33 fields · synced Jun 6, 2026