FDA UDI
In Commercial Distribution
🇺🇸 United States
Gelfoam
DI: 10300090342019
·
Model: Size 100
·
PHARMACIA & UPJOHN COMPANY LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1
Basic Information
- Brand Name
- Gelfoam
- Primary DI
- 10300090342019
- Version / Model
- Size 100
- Company Name
- PHARMACIA & UPJOHN COMPANY LLC
- Labeler DUNS
- 618054084
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2014-09-01
- Public Version
- 6
- Public Version Date
- 2020-12-17
- Public Version Status
- Update
- Public Device Record Key
- 305e42c7-2b57-46a4-8ea1-4d8831718c2b
Device Description
Absorbable Hemostatic Sponge, Collagen Based
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- Yes
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- MR Safe
- Direct Marking Exempt
- Yes
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- No
- Has Expiration Date
- Yes
- Has Donation ID
- No
Sterilization
- Is Sterile
- Yes
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| LMF | Agent, absorbable hemostatic, collagen based | General, Plastic Surgery | 878.4490 | 3 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 47201 | Collagen haemostatic agent, non-antimicrobial | A bioabsorbable device derived from animal collagen (e.g., bovine or porcine collagen) designed to produce a rapid haemostasis through platelet activation/aggregation (which initiates the haemostatic cascade leading to a fibrin clot) during a surgical procedure. It is applied directly to the wound where it remains to be absorbed by the body; it is not dedicated to a specific anatomy/application and does not contain an antimicrobial agent. It may be supplied as a fibrillar or soft, pliable pad/sponge or loose fibres; it may be applied in combination with fibrin adhesives. This is a single-use device. | Yes | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Package | 00300090342012 | GS1 | Carton | 6 | In Commercial Distribution | |
| Primary | 10300090342019 | GS1 |
Customer Contacts
- Phone
- +1(484)865-6166
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| N18286 | 017 |
| N18286 | 018 |
| N18286 | 020 |
| N18286 | 021 |
| N18286 | 023 |
| N18286 | 024 |
| N18286 | 025 |
| N18286 | 026 |
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Width | 80 | Millimeter | |
| Height | 10 | Millimeter | |
| Length | 125 | Millimeter |
Storage Conditions
- Type
- Special Storage Condition, Specify
- Special Conditions
- See USP Controlled Room Temperature
- Type
- Storage Environment Temperature
- Temperature Range
- 15 – 30 Degrees Celsius